Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1209 |
| ensemblid | ENSG00000104853.16 |
| hgncid | 2087 |
| symbol | CLPTM1 |
| name | CLPTM1 regulator of GABA type A receptor forward trafficking |
| refseq_nuc | NM_001294.4 |
| refseq_prot | NP_001285.1 |
| ensembl_nuc | ENST00000337392.10 |
| ensembl_prot | ENSP00000336994.4 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 44955380 |
| end | 44993341 |
| strand | + |
| ver | v1.2 |
| region | chr19:44955380-44993341 |
| region5000 | chr19:44950380-44998341 |
| regionname0 | CLPTM1_chr19_44955380_44993341 |
| regionname5000 | CLPTM1_chr19_44950380_44998341 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 669 | 365 | 88 | 74 | 154 | 12 | 35 | 118 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | MAAAQ others(664): Show |
chr19 | 44950380 | 44998341 |
| a0002 | 0/0 | 669 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | MAAAQ others(664): Show |
chr19 | 44950380 | 44998341 |
| a0003 | 0/0 | 470 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | MAAAQ others(465): Show |
chr19 | 44950380 | 44998341 |
| a0004 | 0/0 | 669 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | MAAAQ others(664): Show |
chr19 | 44950380 | 44998341 |
| a0005 | 0/0 | 669 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | MAAAQ others(664): Show |
chr19 | 44950380 | 44998341 |
| a0006 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | MAAAQ others(664): Show |
chr19 | 44950380 | 44998341 |
| a0007 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | MAAAQ others(664): Show |
chr19 | 44950380 | 44998341 |
| a0008 | 0/0 | 646 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | MAAAQ others(641): Show |
chr19 | 44950380 | 44998341 |
| a0009 | 0/0 | 669 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | MAAAQ others(664): Show |
chr19 | 44950380 | 44998341 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2007 | 148 | 28 | 23 | 74 | 5 | 17 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0001c0002 | 0/0 | 2007 | 142 | 27 | 36 | 60 | 4 | 15 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0001c0003 | 1/0 | 2007 | 45 | 14 | 9 | 18 | 3 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0001c0004 | 0/0 | 2007 | 6 | 6 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0001c0005 | 0/0 | 2007 | 5 | 4 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0001c0006 | 0/0 | 2007 | 5 | 4 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0001c0007 | 0/0 | 2007 | 2 | 0 | 0 | 2 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0001c0009 | 0/0 | 2007 | 2 | 2 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0001c0010 | 0/0 | 2007 | 2 | 0 | 2 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0001c0011 | 0/0 | 2007 | 2 | 0 | 2 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0001c0012 | 0/0 | 2007 | 2 | 0 | 0 | 0 | 0 | 2 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0001c0013 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0001c0014 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0001c0015 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0001c0018 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0002c0008 | 0/0 | 2007 | 2 | 0 | 0 | 0 | 0 | 2 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0003c0016 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0004c0017 | 0/0 | 2007 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0005c0022 | 0/0 | 2007 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0006c0020 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0007c0021 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0008c0019 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 | ||
| a0009c0023 | 0/0 | 2007 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | ATGGC others(2002): Show |
chr19 | 44950380 | 44998341 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2470 | 136 | 24 | 17 | 72 | 5 | 17 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0001t0003 | 0/0 | 2470 | 6 | 0 | 5 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0001t0006 | 0/0 | 2470 | 3 | 2 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0001t0007 | 0/0 | 2470 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0001t0010 | 0/0 | 2470 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0001t0011 | 0/0 | 2470 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0002t0001 | 0/0 | 2470 | 93 | 21 | 20 | 42 | 2 | 8 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0002t0002 | 0/0 | 2470 | 45 | 6 | 15 | 15 | 2 | 7 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0002t0005 | 0/0 | 2470 | 3 | 0 | 0 | 3 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0002t0009 | 0/0 | 2470 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0003t0001 | 0/0 | 2470 | 40 | 12 | 7 | 18 | 3 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0003t0002 | 1/0 | 2470 | 1 | 0 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0003t0004 | 0/0 | 2470 | 4 | 2 | 2 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0004t0001 | 0/0 | 2470 | 6 | 6 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0005t0001 | 0/0 | 2470 | 5 | 4 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0006t0001 | 0/0 | 2470 | 5 | 4 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0007t0001 | 0/0 | 2470 | 2 | 0 | 0 | 2 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0009t0001 | 0/0 | 2470 | 2 | 2 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0010t0001 | 0/0 | 2470 | 2 | 0 | 2 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0011t0001 | 0/0 | 2470 | 2 | 0 | 2 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0012t0001 | 0/0 | 2470 | 2 | 0 | 0 | 0 | 0 | 2 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0013t0001 | 0/0 | 2470 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0014t0002 | 0/0 | 2470 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0015t0001 | 0/0 | 2470 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0001c0018t0002 | 0/0 | 2470 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0002c0008t0002 | 0/0 | 2470 | 2 | 0 | 0 | 0 | 0 | 2 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0003c0016t0008 | 0/0 | 2470 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0004c0017t0001 | 0/0 | 2470 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0005c0022t0001 | 0/0 | 2470 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0006c0020t0001 | 0/0 | 2470 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0007c0021t0001 | 0/0 | 2470 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0008c0019t0001 | 0/0 | 2470 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| a0009c0023t0001 | 0/0 | 2470 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | GACCC others(2465): Show |
chr19 | 44950380 | 44998341 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0277 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0006g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0007g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0010g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0001t0011g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0001 | 0/0 | 6 | 0 | 3 | 2 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0010 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0002t0009g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0003 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0009 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0002g0161 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0003t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0004t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0004t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0004t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0005t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0005t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0005t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0005t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0005t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0006t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0006t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0006t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0006t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0006t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0007t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0007t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0009t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0009t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0010t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0010t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0011t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0011t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0012t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0012t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0013t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0014t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0015t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0001c0018t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0002c0008t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0002c0008t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0003c0016t0008g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0004c0017t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0005c0022t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0006c0020t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0007c0021t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0008c0019t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| a0009c0023t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0149 | EUR | GBR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0009 | EUR | GBR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0084 | EUR | GBR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0010 | EUR | FIN | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0082 | EUR | FIN | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0281 | EUR | FIN | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | CHS | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | CHS | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | CHS | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00609 | hp2 | a0001 | c0003 | t0001 | g0008 | EAS | CHS | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | CHS | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0196 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0164 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00738 | hp2 | a0001 | c0006 | t0001 | g0034 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0133 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0132 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0257 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0083 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0073 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0089 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0069 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0192 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0175 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01099 | hp1 | a0001 | c0003 | t0004 | g0102 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0145 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01109 | hp2 | a0001 | c0003 | t0004 | g0101 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0194 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0108 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0128 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | PUR | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0117 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01257 | hp1 | a0001 | c0010 | t0001 | g0292 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0018 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01258 | hp2 | a0001 | c0010 | t0001 | g0289 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0150 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0274 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0039 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0162 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0009 | EUR | IBS | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | IBS | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0009 | EUR | IBS | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0098 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0116 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0193 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01975 | hp2 | a0001 | c0002 | t0009 | g0195 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01978 | hp1 | a0001 | c0011 | t0001 | g0109 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0088 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01981 | hp2 | a0001 | c0011 | t0001 | g0022 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0065 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0086 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | KHV | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | KHV | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | KHV | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02055 | hp1 | a0001 | c0001 | t0011 | g0211 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02055 | hp2 | a0001 | c0005 | t0001 | g0205 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | KHV | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | KHV | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0167 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0099 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02148 | hp1 | a0001 | c0003 | t0001 | g0022 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | CDX | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CDX | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02165 | hp2 | a0001 | c0003 | t0001 | g0197 | EAS | CDX | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0040 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0018 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02273 | hp2 | a0001 | c0003 | t0001 | g0003 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02293 | hp1 | a0001 | c0003 | t0001 | g0003 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0266 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0003 | AMR | PEL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02451 | hp1 | a0001 | c0004 | t0001 | g0017 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | KHV | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02572 | hp1 | a0003 | c0016 | t0008 | g0313 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02572 | hp2 | a0001 | c0006 | t0001 | g0031 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02602 | hp1 | a0001 | c0018 | t0002 | g0071 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0077 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0100 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0076 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02622 | hp1 | a0001 | c0013 | t0001 | g0180 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02622 | hp2 | a0001 | c0006 | t0001 | g0032 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0079 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0127 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02683 | hp1 | a0004 | c0017 | t0001 | g0148 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02723 | hp1 | a0001 | c0004 | t0001 | g0058 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02809 | hp1 | a0001 | c0006 | t0001 | g0029 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0021 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0020 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02818 | hp2 | a0001 | c0003 | t0004 | g0104 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0021 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0106 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0185 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0183 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0105 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0097 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0129 | AFR | ESN | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0184 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03098 | hp2 | a0001 | c0004 | t0001 | g0056 | AFR | MSL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03130 | hp1 | a0001 | c0009 | t0001 | g0201 | AFR | ESN | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0067 | AFR | ESN | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | ESN | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0152 | AFR | ESN | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0166 | AFR | MSL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0146 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03453 | hp2 | a0001 | c0014 | t0002 | g0062 | AFR | MSL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03486 | hp1 | a0005 | c0022 | t0001 | g0170 | AFR | MSL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0066 | AFR | MSL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03490 | hp1 | a0002 | c0008 | t0002 | g0075 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03492 | hp2 | a0002 | c0008 | t0002 | g0070 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | ESN | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | ESN | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0095 | AFR | GWD | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0096 | AFR | MSL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0064 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0063 | SAS | STU | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03688 | hp2 | a0001 | c0012 | t0001 | g0119 | SAS | STU | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0080 | SAS | PJL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0143 | SAS | BEB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | BEB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0142 | SAS | BEB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG04199 | hp1 | a0001 | c0012 | t0001 | g0118 | SAS | STU | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0190 | SAS | STU | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0178 | SAS | STU | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0074 | SAS | STU | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | STU | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0177 | SAS | STU | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | YRI | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18522 | hp2 | a0001 | c0003 | t0004 | g0103 | AFR | YRI | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | CHB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18906 | hp1 | a0001 | c0006 | t0001 | g0030 | AFR | YRI | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | YRI | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18941 | hp1 | a0001 | c0003 | t0001 | g0113 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18952 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18953 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18954 | hp2 | a0001 | c0003 | t0001 | g0114 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18968 | hp1 | a0006 | c0020 | t0001 | g0244 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18968 | hp2 | a0001 | c0003 | t0001 | g0111 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18973 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18975 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18978 | hp1 | a0001 | c0003 | t0001 | g0120 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18984 | hp1 | a0001 | c0003 | t0001 | g0107 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18984 | hp2 | a0007 | c0021 | t0001 | g0286 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18985 | hp2 | a0001 | c0003 | t0001 | g0123 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18986 | hp1 | a0008 | c0019 | t0001 | g0224 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18987 | hp2 | a0001 | c0001 | t0007 | g0310 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18991 | hp2 | a0001 | c0003 | t0001 | g0121 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18993 | hp1 | a0001 | c0003 | t0001 | g0122 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18995 | hp2 | a0001 | c0007 | t0001 | g0131 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18997 | hp1 | a0001 | c0002 | t0002 | g0311 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18999 | hp1 | a0001 | c0002 | t0005 | g0026 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19011 | hp2 | a0001 | c0007 | t0001 | g0141 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0078 | AFR | LWK | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19043 | hp1 | a0001 | c0005 | t0001 | g0033 | AFR | LWK | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19043 | hp2 | a0001 | c0004 | t0001 | g0049 | AFR | LWK | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19059 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19062 | hp1 | a0009 | c0023 | t0001 | g0284 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19081 | hp2 | a0001 | c0002 | t0005 | g0151 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19083 | hp1 | a0001 | c0003 | t0001 | g0110 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19084 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19088 | hp2 | a0001 | c0003 | t0001 | g0112 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19089 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19091 | hp1 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0041 | AFR | YRI | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA20129 | hp1 | a0001 | c0005 | t0001 | g0202 | AFR | ASW | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0085 | SAS | GIH | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0068 | SAS | GIH | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0087 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG01123 | hp2 | a0001 | c0005 | t0001 | g0203 | AMR | CLM | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02109 | hp1 | a0001 | c0009 | t0001 | g0200 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02109 | hp2 | a0001 | c0004 | t0001 | g0017 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02486 | hp1 | a0001 | c0005 | t0001 | g0204 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | ACB | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0057 | AFR | MSL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0072 | AFR | USA | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0182 | AFR | USA | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | USA | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA20300 | hp2 | a0001 | c0015 | t0001 | g0199 | AFR | USA | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | LWK | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0191 | AFR | LWK | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0277 | REF | REF | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0002 | g0161 | REF | REF | CLPTM1_chr19_44950380_44998341 | CLPTM1 | chr19 | 44950380 | 44998341 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:44977430 | C | T | 1 | a0005 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.556C>T | p.Arg186Cys | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/14 | 572/2470 | 556/2010 | 186/669 | chr19 | 44977430 | |||
| chr19:44986563 | C | T | 1 | a0003 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.781C>T | p.Pro261Ser | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/14 | 797/2470 | 781/2010 | 261/669 | chr19 | 44986563 | |||
| chr19:44986567 | T | C | 1 | a0003 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.785T>C | p.Leu262Pro | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/14 | 801/2470 | 785/2010 | 262/669 | chr19 | 44986567 | |||
| chr19:44986571 | T | G | 1 | a0003 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.789T>G | p.Asp263Glu | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/14 | 805/2470 | 789/2010 | 263/669 | chr19 | 44986571 | |||
| chr19:44990416 | G | T | 1 | a0007 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.1154G>T | p.Arg385Leu | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 10/14 | 1170/2470 | 1154/2010 | 385/669 | chr19 | 44990416 | |||
| chr19:44990487 | T | G | 1 | a0003 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1225T>G | p.Tyr409Asp | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 10/14 | 1241/2470 | 1225/2010 | 409/669 | chr19 | 44990487 | |||
| chr19:44990491 | T | G | 1 | a0003 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1229T>G | p.Ile410Ser | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 10/14 | 1245/2470 | 1229/2010 | 410/669 | chr19 | 44990491 | |||
| chr19:44990541 | G | T | 1 | a0007 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.1279G>T | p.Val427Phe | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 10/14 | 1295/2470 | 1279/2010 | 427/669 | chr19 | 44990541 | |||
| chr19:44990542 | T | C | 1 | a0007 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.1280T>C | p.Val427Ala | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 10/14 | 1296/2470 | 1280/2010 | 427/669 | chr19 | 44990542 | |||
| chr19:44990544 | C | G | 1 | a0007 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.1282C>G | p.Leu428Val | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 10/14 | 1298/2470 | 1282/2010 | 428/669 | chr19 | 44990544 | |||
| chr19:44990545 | T | G | 1 | a0003 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1283T>G | p.Leu428Arg | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 10/14 | 1299/2470 | 1283/2010 | 428/669 | chr19 | 44990545 | |||
| chr19:44990584 | G | A | 1 | a0002 | 2 | HG03490.hp1 HG03492.hp2 |
missense_variant&splice_region_variant | MODERATE | c.1322G>A | p.Arg441Gln | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 10/14 | 1338/2470 | 1322/2010 | 441/669 | chr19 | 44990584 | |||
| chr19:44990935 | T | G | 1 | a0003 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1409T>G | p.Val470Gly | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 11/14 | 1425/2470 | 1409/2010 | 470/669 | chr19 | 44990935 | |||
| chr19:44990939 | T | A | 1 | a0003 | 1 | HG02572.hp1 | stop_gained | HIGH | c.1413T>A | p.Tyr471* | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 11/14 | 1429/2470 | 1413/2010 | 471/669 | chr19 | 44990939 | |||
| chr19:44991302 | T | G | 1 | a0003 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1484T>G | p.Leu495Arg | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 12/14 | 1500/2470 | 1484/2010 | 495/669 | chr19 | 44991302 | |||
| chr19:44992241 | A | C | 1 | a0006 | 1 | NA18968.hp1 | missense_variant | MODERATE | c.1564A>C | p.Thr522Pro | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 13/14 | 1580/2470 | 1564/2010 | 522/669 | chr19 | 44992241 | |||
| chr19:44992275 | T | G | 1 | a0003 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1598T>G | p.Leu533Arg | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 13/14 | 1614/2470 | 1598/2010 | 533/669 | chr19 | 44992275 | |||
| chr19:44992325 | A | T | 1 | a0009 | 1 | NA19062.hp1 | missense_variant | MODERATE | c.1648A>T | p.Asn550Tyr | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 13/14 | 1664/2470 | 1648/2010 | 550/669 | chr19 | 44992325 | |||
| chr19:44992382 | A | C | 1 | a0003 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1705A>C | p.Ile569Leu | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 13/14 | 1721/2470 | 1705/2010 | 569/669 | chr19 | 44992382 | |||
| chr19:44992614 | T | G | 1 | a0003 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1727T>G | p.Val576Gly | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 1743/2470 | 1727/2010 | 576/669 | chr19 | 44992614 | |||
| chr19:44992617 | T | G | 1 | a0003 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1730T>G | p.Val577Gly | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 1746/2470 | 1730/2010 | 577/669 | chr19 | 44992617 | |||
| chr19:44992826 | C | T | 1 | a0008 | 1 | NA18986.hp1 | stop_gained | HIGH | c.1939C>T | p.Gln647* | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 1955/2470 | 1939/2010 | 647/669 | chr19 | 44992826 | |||
| chr19:44992875 | C | G | 1 | a0004 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.1988C>G | p.Ala663Gly | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 2004/2470 | 1988/2010 | 663/669 | chr19 | 44992875 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:44961965 | G | A | 1 | a0001c0013 | 1 | HG02622.hp1 | splice_region_variant&synonymous_variant | LOW | c.75G>A | p.Val25Val | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/14 | 91/2470 | 75/2010 | 25/669 | chr19 | 44961965 | |||
| chr19:44962025 | G | A | 1 | a0001c0014 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.135G>A | p.Pro45Pro | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/14 | 151/2470 | 135/2010 | 45/669 | chr19 | 44962025 | |||
| chr19:44973156 | C | T | 1 | a0001c0006 | 5 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
synonymous_variant | LOW | c.255C>T | p.Pro85Pro | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/14 | 271/2470 | 255/2010 | 85/669 | chr19 | 44973156 | |||
| chr19:44973165 | T | C | 20 | a0001c0001 a0001c0002 a0001c0004 others(17): Show |
324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
synonymous_variant | LOW | c.264T>C | p.Ala88Ala | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/14 | 280/2470 | 264/2010 | 88/669 | chr19 | 44973165 | |||
| chr19:44974492 | G | A | 1 | a0001c0015 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.363G>A | p.Thr121Thr | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/14 | 379/2470 | 363/2010 | 121/669 | chr19 | 44974492 | |||
| chr19:44977348 | C | T | 1 | a0009c0023 | 1 | NA19062.hp1 | synonymous_variant | LOW | c.474C>T | p.Val158Val | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/14 | 490/2470 | 474/2010 | 158/669 | chr19 | 44977348 | |||
| chr19:44986562 | T | C | 1 | a0003c0016 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.780T>C | p.Pro260Pro | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/14 | 796/2470 | 780/2010 | 260/669 | chr19 | 44986562 | |||
| chr19:44987312 | A | G | 10 | a0001c0001 a0001c0004 a0001c0006 others(7): Show |
167 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(164): Show |
synonymous_variant | LOW | c.927A>G | p.Pro309Pro | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 8/14 | 943/2470 | 927/2010 | 309/669 | chr19 | 44987312 | |||
| chr19:44987378 | T | C | 9 | a0001c0002 a0001c0007 a0001c0013 others(6): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
synonymous_variant | LOW | c.993T>C | p.Gly331Gly | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 8/14 | 1009/2470 | 993/2010 | 331/669 | chr19 | 44987378 | |||
| chr19:44987385 | T | C | 1 | a0001c0007 | 2 | NA18995.hp2 NA19011.hp2 |
synonymous_variant | LOW | c.1000T>C | p.Leu334Leu | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 8/14 | 1016/2470 | 1000/2010 | 334/669 | chr19 | 44987385 | |||
| chr19:44988115 | G | A | 1 | a0001c0011 | 2 | HG01978.hp1 HG01981.hp2 |
synonymous_variant | LOW | c.1074G>A | p.Ala358Ala | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/14 | 1090/2470 | 1074/2010 | 358/669 | chr19 | 44988115 | |||
| chr19:44990546 | C | T | 1 | a0001c0004 | 6 | HG02109.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
synonymous_variant | LOW | c.1284C>T | p.Leu428Leu | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 10/14 | 1300/2470 | 1284/2010 | 428/669 | chr19 | 44990546 | |||
| chr19:44991276 | C | T | 1 | a0001c0010 | 2 | HG01257.hp1 HG01258.hp2 |
synonymous_variant | LOW | c.1458C>T | p.Leu486Leu | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 12/14 | 1474/2470 | 1458/2010 | 486/669 | chr19 | 44991276 | |||
| chr19:44992321 | C | T | 1 | a0001c0009 | 2 | HG02109.hp1 HG03130.hp1 |
synonymous_variant | LOW | c.1644C>T | p.Ala548Ala | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 13/14 | 1660/2470 | 1644/2010 | 548/669 | chr19 | 44992321 | |||
| chr19:44992654 | C | T | 1 | a0001c0018 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.1767C>T | p.Arg589Arg | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 1783/2470 | 1767/2010 | 589/669 | chr19 | 44992654 | |||
| chr19:44992717 | C | T | 1 | a0004c0017 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.1830C>T | p.Pro610Pro | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 1846/2470 | 1830/2010 | 610/669 | chr19 | 44992717 | |||
| chr19:44992771 | C | T | 1 | a0001c0012 | 2 | HG03688.hp2 HG04199.hp1 |
synonymous_variant | LOW | c.1884C>T | p.Thr628Thr | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 1900/2470 | 1884/2010 | 628/669 | chr19 | 44992771 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:44993002 | G | C | 1 | a0001c0001t0007 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*105G>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 105 | chr19 | 44993002 | ||||||
| chr19:44993003 | G | A | 1 | a0001c0001t0007 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*106G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 106 | chr19 | 44993003 | ||||||
| chr19:44993006 | C | G | 1 | a0001c0001t0007 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*109C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 109 | chr19 | 44993006 | ||||||
| chr19:44993007 | G | A | 1 | a0001c0001t0007 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*110G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 110 | chr19 | 44993007 | ||||||
| chr19:44993008 | G | A | 1 | a0001c0001t0007 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*111G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 111 | chr19 | 44993008 | ||||||
| chr19:44993009 | T | A | 1 | a0001c0001t0007 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*112T>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 112 | chr19 | 44993009 | ||||||
| chr19:44993013 | A | C | 1 | a0001c0001t0007 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*116A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 116 | chr19 | 44993013 | ||||||
| chr19:44993019 | G | A | 1 | a0003c0016t0008 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*122G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 122 | chr19 | 44993019 | ||||||
| chr19:44993027 | T | G | 1 | a0001c0001t0007 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*130T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 130 | chr19 | 44993027 | ||||||
| chr19:44993045 | T | C | 28 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(25): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*148T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 148 | chr19 | 44993045 | ||||||
| chr19:44993047 | T | A | 1 | a0001c0001t0007 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*150T>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 150 | chr19 | 44993047 | ||||||
| chr19:44993048 | A | G | 1 | a0001c0001t0007 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*151A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 151 | chr19 | 44993048 | ||||||
| chr19:44993055 | G | A | 1 | a0001c0002t0005 | 3 | NA18973.hp1 NA18999.hp1 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*158G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 158 | chr19 | 44993055 | ||||||
| chr19:44993124 | G | A | 1 | a0001c0003t0004 | 4 | HG01099.hp1 HG01109.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*227G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 227 | chr19 | 44993124 | ||||||
| chr19:44993171 | C | T | 1 | a0001c0001t0003 | 6 | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*274C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 274 | chr19 | 44993171 | ||||||
| chr19:44993177 | C | T | 1 | a0001c0001t0011 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*280C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 280 | chr19 | 44993177 | ||||||
| chr19:44993184 | G | T | 1 | a0001c0001t0006 | 3 | HG01243.hp2 NA18906.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*287G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 287 | chr19 | 44993184 | ||||||
| chr19:44993207 | G | A | 1 | a0001c0002t0005 | 3 | NA18973.hp1 NA18999.hp1 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*310G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 310 | chr19 | 44993207 | ||||||
| chr19:44993214 | C | G | 1 | a0001c0001t0010 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*317C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 317 | chr19 | 44993214 | ||||||
| chr19:44993253 | G | A | 1 | a0001c0002t0009 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*356G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 14/14 | 356 | chr19 | 44993253 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:44955537 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.72+70C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44955537 | |||||||
| chr19:44955668 | C | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(116): Show |
136 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.72+201C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44955668 | |||||||
| chr19:44955762 | G | GTACA | 4 | a0001c0005t0001g0202 a0001c0005t0001g0203 a0001c0005t0001g0204 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+295_72+296insTA others(2): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44955762 | |||||||
| chr19:44955763 | G | A | 4 | a0001c0005t0001g0202 a0001c0005t0001g0203 a0001c0005t0001g0204 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+296G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44955763 | |||||||
| chr19:44955764 | T | C | 4 | a0001c0005t0001g0202 a0001c0005t0001g0203 a0001c0005t0001g0204 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+297T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44955764 | |||||||
| chr19:44955765 | T | G | 4 | a0001c0005t0001g0202 a0001c0005t0001g0203 a0001c0005t0001g0204 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+298T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44955765 | |||||||
| chr19:44955825 | C | T | 2 | a0001c0001t0001g0314 a0001c0001t0001g0315 |
2 | HG00738.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.72+358C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44955825 | |||||||
| chr19:44955835 | T | C | 6 | a0001c0005t0001g0033 a0001c0006t0001g0029 a0001c0006t0001g0030 others(3): Show |
6 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+368T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44955835 | |||||||
| chr19:44955960 | T | C | 6 | a0001c0005t0001g0033 a0001c0006t0001g0029 a0001c0006t0001g0030 others(3): Show |
6 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+493T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44955960 | |||||||
| chr19:44956039 | G | A | 4 | a0001c0002t0002g0035 a0001c0002t0002g0036 a0001c0002t0002g0037 others(1): Show |
4 | NA18963.hp1 NA18994.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+572G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44956039 | |||||||
| chr19:44956096 | C | T | 2 | a0001c0009t0001g0200 a0001c0009t0001g0201 |
2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.72+629C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44956096 | |||||||
| chr19:44956103 | C | T | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.72+636C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44956103 | |||||||
| chr19:44956239 | A | G | 1 | a0001c0015t0001g0199 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.72+772A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44956239 | |||||||
| chr19:44956414 | G | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(194): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.72+947G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44956414 | |||||||
| chr19:44956414 | G | T | 1 | a0001c0002t0001g0198 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.72+947G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44956414 | |||||||
| chr19:44956594 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(194): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.72+1127T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44956594 | |||||||
| chr19:44956624 | T | C | 2 | a0001c0002t0002g0035 a0001c0002t0002g0036 |
2 | NA18963.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.72+1157T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44956624 | |||||||
| chr19:44956819 | A | T | 1 | a0001c0003t0001g0197 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.72+1352A>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44956819 | |||||||
| chr19:44956956 | G | T | 1 | a0001c0003t0001g0095 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.72+1489G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44956956 | |||||||
| chr19:44956997 | G | A | 1 | a0001c0002t0002g0039 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.72+1530G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44956997 | |||||||
| chr19:44957255 | A | C | 6 | a0001c0005t0001g0033 a0001c0006t0001g0029 a0001c0006t0001g0030 others(3): Show |
6 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+1788A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44957255 | |||||||
| chr19:44957292 | TTGAC | T | 43 | a0001c0002t0002g0005 a0001c0002t0002g0018 a0001c0002t0002g0019 others(40): Show |
48 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.72+1828_72+1831del others(4): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 44957292 | ||||||
| chr19:44957409 | C | A | 1 | a0001c0001t0001g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.72+1942C>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44957409 | |||||||
| chr19:44957435 | G | C | 14 | a0001c0001t0001g0011 a0001c0001t0001g0206 a0001c0001t0001g0207 others(11): Show |
16 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.72+1968G>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44957435 | |||||||
| chr19:44957507 | G | A | 235 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(232): Show |
271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.72+2040G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44957507 | |||||||
| chr19:44957750 | A | G | 4 | a0001c0002t0001g0193 a0001c0002t0001g0194 a0001c0002t0001g0196 others(1): Show |
4 | HG00639.hp1 HG01168.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+2283A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44957750 | |||||||
| chr19:44958085 | G | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(121): Show |
141 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.72+2618G>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44958085 | |||||||
| chr19:44958162 | G | A | 1 | a0001c0002t0002g0061 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.72+2695G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44958162 | |||||||
| chr19:44958333 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.72+2866T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44958333 | |||||||
| chr19:44958413 | C | A | 1 | a0001c0002t0002g0061 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.72+2946C>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44958413 | |||||||
| chr19:44958414 | G | C | 1 | a0001c0002t0002g0061 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.72+2947G>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44958414 | |||||||
| chr19:44958526 | C | T | 6 | a0001c0005t0001g0033 a0001c0006t0001g0029 a0001c0006t0001g0030 others(3): Show |
6 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+3059C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44958526 | |||||||
| chr19:44958703 | C | T | 1 | a0001c0002t0001g0059 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.72+3236C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44958703 | |||||||
| chr19:44958723 | C | T | 23 | a0001c0003t0001g0003 a0001c0003t0001g0008 a0001c0003t0001g0009 others(20): Show |
32 | HG00099.hp2 HG00609.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.73-3240C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44958723 | |||||||
| chr19:44958739 | A | G | 39 | a0001c0002t0001g0191 a0001c0002t0001g0192 a0001c0003t0001g0003 others(36): Show |
50 | HG00099.hp2 HG00609.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.73-3224A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44958739 | |||||||
| chr19:44958828 | T | A | 1 | a0001c0006t0001g0029 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.73-3135T>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44958828 | |||||||
| chr19:44958832 | C | T | 2 | a0001c0002t0001g0190 a0001c0006t0001g0029 |
2 | HG02809.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.73-3131C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44958832 | |||||||
| chr19:44958833 | C | A | 1 | a0001c0006t0001g0029 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.73-3130C>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44958833 | |||||||
| chr19:44958836 | A | G | 1 | a0001c0006t0001g0029 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.73-3127A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44958836 | |||||||
| chr19:44958907 | T | C | 1 | a0001c0014t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.73-3056T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44958907 | |||||||
| chr19:44958923 | C | G | 3 | a0001c0002t0001g0187 a0001c0002t0001g0188 a0001c0002t0001g0189 |
3 | NA19000.hp2 NA19004.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.73-3040C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44958923 | |||||||
| chr19:44959006 | C | T | 6 | a0001c0005t0001g0033 a0001c0006t0001g0029 a0001c0006t0001g0030 others(3): Show |
6 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.73-2957C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44959006 | |||||||
| chr19:44959021 | G | A | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.73-2942G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44959021 | |||||||
| chr19:44959052 | C | T | 4 | a0001c0004t0001g0017 a0001c0004t0001g0056 a0001c0004t0001g0057 others(1): Show |
5 | HG02109.hp2 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-2911C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44959052 | |||||||
| chr19:44959414 | G | A | 4 | a0001c0006t0001g0029 a0001c0006t0001g0030 a0001c0006t0001g0031 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-2549G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44959414 | |||||||
| chr19:44959429 | A | G | 1 | a0001c0002t0001g0186 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.73-2534A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44959429 | |||||||
| chr19:44959657 | C | T | 6 | a0001c0005t0001g0033 a0001c0006t0001g0029 a0001c0006t0001g0030 others(3): Show |
6 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.73-2306C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44959657 | |||||||
| chr19:44959790 | A | G | 6 | a0001c0005t0001g0033 a0001c0006t0001g0029 a0001c0006t0001g0030 others(3): Show |
6 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.73-2173A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44959790 | |||||||
| chr19:44959831 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.73-2132T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44959831 | |||||||
| chr19:44959861 | T | C | 6 | a0001c0005t0001g0033 a0001c0006t0001g0029 a0001c0006t0001g0030 others(3): Show |
6 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.73-2102T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44959861 | |||||||
| chr19:44959902 | T | C | 2 | a0001c0001t0006g0015 a0001c0001t0006g0041 |
3 | HG01243.hp2 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.73-2061T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44959902 | |||||||
| chr19:44959923 | A | G | 7 | a0001c0002t0002g0019 a0001c0002t0002g0061 a0001c0002t0002g0090 others(4): Show |
8 | HG00621.hp2 NA18955.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.73-2040A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44959923 | |||||||
| chr19:44959999 | C | G | 20 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0044 others(17): Show |
22 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.73-1964C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44959999 | |||||||
| chr19:44960128 | C | T | 23 | a0001c0003t0001g0003 a0001c0003t0001g0008 a0001c0003t0001g0009 others(20): Show |
32 | HG00099.hp2 HG00609.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.73-1835C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44960128 | |||||||
| chr19:44960129 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02738.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.73-1834G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44960129 | |||||||
| chr19:44960187 | G | A | 1 | a0001c0005t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.73-1776G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44960187 | |||||||
| chr19:44960193 | C | T | 1 | a0001c0001t0001g0312 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.73-1770C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44960193 | |||||||
| chr19:44960234 | C | T | 1 | a0001c0002t0002g0089 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.73-1729C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44960234 | |||||||
| chr19:44960260 | A | G | 1 | a0001c0002t0001g0196 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.73-1703A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44960260 | |||||||
| chr19:44960282 | C | T | 6 | a0001c0005t0001g0033 a0001c0006t0001g0029 a0001c0006t0001g0030 others(3): Show |
6 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.73-1681C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44960282 | |||||||
| chr19:44960283 | T | A | 23 | a0001c0003t0001g0003 a0001c0003t0001g0008 a0001c0003t0001g0009 others(20): Show |
32 | HG00099.hp2 HG00609.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.73-1680T>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44960283 | |||||||
| chr19:44960309 | T | C | 6 | a0001c0005t0001g0033 a0001c0006t0001g0029 a0001c0006t0001g0030 others(3): Show |
6 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.73-1654T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44960309 | |||||||
| chr19:44960409 | G | C | 1 | a0001c0001t0001g0220 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.73-1554G>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44960409 | |||||||
| chr19:44960444 | G | A | 6 | a0001c0005t0001g0033 a0001c0006t0001g0029 a0001c0006t0001g0030 others(3): Show |
6 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.73-1519G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44960444 | |||||||
| chr19:44960477 | C | T | 6 | a0001c0005t0001g0033 a0001c0006t0001g0029 a0001c0006t0001g0030 others(3): Show |
6 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.73-1486C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44960477 | |||||||
| chr19:44960629 | A | G | 3 | a0001c0002t0001g0007 a0001c0002t0001g0027 a0001c0002t0001g0185 |
7 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-1334A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44960629 | |||||||
| chr19:44960883 | CTG | C | 6 | a0001c0005t0001g0033 a0001c0006t0001g0029 a0001c0006t0001g0030 others(3): Show |
6 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.73-1079_73-1078del others(2): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44960883 | |||||||
| chr19:44960933 | G | A | 6 | a0001c0005t0001g0033 a0001c0006t0001g0029 a0001c0006t0001g0030 others(3): Show |
6 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.73-1030G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44960933 | |||||||
| chr19:44960972 | C | T | 1 | a0001c0002t0001g0059 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.73-991C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44960972 | |||||||
| chr19:44961024 | G | A | 4 | a0001c0005t0001g0202 a0001c0005t0001g0203 a0001c0005t0001g0204 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-939G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44961024 | |||||||
| chr19:44961102 | T | C | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.73-861T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44961102 | |||||||
| chr19:44961214 | C | CA | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG02683.hp2 HG03239.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.73-748dupA | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 44961214 | ||||||
| chr19:44961452 | T | G | 1 | a0001c0001t0001g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.73-511T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44961452 | |||||||
| chr19:44961684 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.73-279G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44961684 | |||||||
| chr19:44961706 | C | T | 43 | a0001c0002t0002g0005 a0001c0002t0002g0018 a0001c0002t0002g0019 others(40): Show |
48 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.73-257C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44961706 | |||||||
| chr19:44961725 | A | G | 1 | a0001c0015t0001g0199 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.73-238A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44961725 | |||||||
| chr19:44961927 | A | G | 5 | a0001c0005t0001g0202 a0001c0005t0001g0203 a0001c0005t0001g0204 others(2): Show |
5 | HG01123.hp2 HG02055.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-36A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 1/13 | chr19 | 44961927 | |||||||
| chr19:44962106 | GA | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(160): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.185+35delA | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44962106 | ||||||
| chr19:44962112 | A | G | 7 | a0001c0003t0001g0100 a0001c0003t0001g0105 a0001c0003t0001g0106 others(4): Show |
7 | HG01099.hp1 HG01109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+37A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44962112 | |||||||
| chr19:44962164 | G | A | 1 | a0001c0002t0001g0124 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.185+89G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44962164 | |||||||
| chr19:44962198 | C | CT | 15 | a0001c0002t0001g0010 a0001c0002t0001g0184 a0001c0002t0001g0191 others(12): Show |
17 | HG00280.hp2 HG00738.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.185+134dupT | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44962198 | ||||||
| chr19:44962217 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.185+142G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44962217 | |||||||
| chr19:44962381 | G | A | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.185+306G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44962381 | |||||||
| chr19:44962536 | T | C | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.185+461T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44962536 | |||||||
| chr19:44962561 | G | A | 1 | a0001c0003t0001g0107 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.185+486G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44962561 | |||||||
| chr19:44962645 | C | G | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.185+570C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44962645 | |||||||
| chr19:44962801 | T | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(195): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.185+726T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44962801 | |||||||
| chr19:44962887 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(194): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.185+812T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44962887 | |||||||
| chr19:44962929 | A | G | 9 | a0001c0005t0001g0033 a0001c0005t0001g0202 a0001c0005t0001g0203 others(6): Show |
9 | HG00738.hp2 HG01123.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.185+854A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44962929 | |||||||
| chr19:44962950 | G | A | 37 | a0001c0003t0001g0003 a0001c0003t0001g0008 a0001c0003t0001g0009 others(34): Show |
48 | HG00099.hp2 HG00609.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.185+875G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44962950 | |||||||
| chr19:44962981 | C | T | 37 | a0001c0003t0001g0003 a0001c0003t0001g0008 a0001c0003t0001g0009 others(34): Show |
48 | HG00099.hp2 HG00609.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.185+906C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44962981 | |||||||
| chr19:44962985 | A | G | 6 | a0001c0001t0001g0042 a0001c0001t0006g0015 a0001c0001t0006g0041 others(3): Show |
7 | HG01243.hp2 HG02109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+910A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44962985 | |||||||
| chr19:44963042 | C | CA | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(115): Show |
135 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.185+975dupA | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44963042 | ||||||
| chr19:44963042 | CA | C | 9 | a0001c0005t0001g0033 a0001c0005t0001g0202 a0001c0005t0001g0203 others(6): Show |
9 | HG00738.hp2 HG01123.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.185+975delA | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44963042 | ||||||
| chr19:44963068 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(194): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.185+993T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44963068 | |||||||
| chr19:44963078 | C | T | 29 | a0001c0003t0001g0003 a0001c0003t0001g0008 a0001c0003t0001g0009 others(26): Show |
40 | HG00099.hp2 HG00609.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.185+1003C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44963078 | |||||||
| chr19:44963099 | TCAGGAGG others(7): Show |
T | 1 | a0001c0002t0001g0126 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.185+1031_185+1044d others(16): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44963099 | ||||||
| chr19:44963111 | G | T | 4 | a0001c0006t0001g0029 a0001c0006t0001g0031 a0001c0006t0001g0032 others(1): Show |
4 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+1036G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44963111 | |||||||
| chr19:44963150 | G | A | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.185+1075G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44963150 | |||||||
| chr19:44963207 | C | CA | 74 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(71): Show |
85 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.185+1153dupA | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44963207 | ||||||
| chr19:44963207 | C | CAA | 12 | a0001c0001t0006g0015 a0001c0001t0010g0040 a0001c0003t0001g0022 others(9): Show |
13 | HG01109.hp2 HG01175.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.185+1152_185+1153d others(4): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44963207 | ||||||
| chr19:44963207 | CA | C | 12 | a0001c0001t0001g0042 a0001c0002t0002g0061 a0001c0002t0002g0063 others(9): Show |
12 | HG00738.hp2 HG01993.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.185+1153delA | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44963207 | ||||||
| chr19:44963207 | CAA | C | 39 | a0001c0002t0002g0005 a0001c0002t0002g0018 a0001c0002t0002g0019 others(36): Show |
44 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.185+1152_185+1153d others(4): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44963207 | ||||||
| chr19:44963328 | A | AT | 6 | a0001c0002t0001g0137 a0001c0002t0001g0138 a0001c0002t0001g0181 others(3): Show |
6 | HG00597.hp2 HG02027.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+1268dupT | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44963328 | ||||||
| chr19:44963328 | A | T | 2 | a0001c0002t0001g0182 a0001c0002t0001g0183 |
2 | HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.185+1253A>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44963328 | |||||||
| chr19:44963328 | AT | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(173): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.185+1268delT | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44963328 | ||||||
| chr19:44963390 | A | G | 9 | a0001c0005t0001g0033 a0001c0005t0001g0202 a0001c0005t0001g0203 others(6): Show |
9 | HG00738.hp2 HG01123.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.185+1315A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44963390 | |||||||
| chr19:44963418 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.185+1343C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44963418 | |||||||
| chr19:44963515 | T | C | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.185+1440T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44963515 | |||||||
| chr19:44963518 | G | C | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.185+1443G>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44963518 | |||||||
| chr19:44963535 | C | A | 59 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0028 others(56): Show |
62 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.185+1460C>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44963535 | |||||||
| chr19:44963564 | A | G | 1 | a0001c0014t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.185+1489A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44963564 | |||||||
| chr19:44963615 | G | A | 1 | a0001c0002t0001g0127 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.185+1540G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44963615 | |||||||
| chr19:44963679 | G | A | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.185+1604G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44963679 | |||||||
| chr19:44963847 | A | G | 3 | a0001c0006t0001g0029 a0001c0006t0001g0031 a0001c0006t0001g0032 |
3 | HG02572.hp2 HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.185+1772A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44963847 | |||||||
| chr19:44963875 | C | T | 11 | a0001c0002t0002g0005 a0001c0002t0002g0018 a0001c0002t0002g0065 others(8): Show |
15 | HG00140.hp2 HG00323.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.185+1800C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44963875 | |||||||
| chr19:44963894 | A | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0206 a0001c0001t0001g0207 others(11): Show |
16 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.185+1819A>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44963894 | |||||||
| chr19:44963933 | C | CT | 38 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0219 others(35): Show |
39 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.185+1872dupT | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44963933 | ||||||
| chr19:44964013 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.185+1938G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44964013 | |||||||
| chr19:44964298 | C | CT | 41 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0051 others(38): Show |
44 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.185+2253dupT | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44964298 | ||||||
| chr19:44964298 | C | CTT | 11 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0006g0041 others(8): Show |
12 | HG01081.hp2 HG01975.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.185+2252_185+2253d others(4): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44964298 | ||||||
| chr19:44964298 | C | CTTTTTTT others(1): Show |
11 | a0001c0002t0002g0018 a0001c0002t0002g0035 a0001c0002t0002g0066 others(8): Show |
12 | HG00323.hp1 HG01069.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.185+2246_185+2253d others(10): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44964298 | ||||||
| chr19:44964298 | C | CTTTTTTT others(2): Show |
13 | a0001c0002t0002g0005 a0001c0002t0002g0019 a0001c0002t0002g0036 others(10): Show |
17 | HG00140.hp2 HG00621.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.185+2245_185+2253d others(11): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44964298 | ||||||
| chr19:44964298 | C | CTTTTTTT others(3): Show |
12 | a0001c0002t0002g0037 a0001c0002t0002g0039 a0001c0002t0002g0061 others(9): Show |
12 | HG01070.hp1 HG01070.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.185+2244_185+2253d others(12): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44964298 | ||||||
| chr19:44964298 | C | CTTTTTTT others(4): Show |
7 | a0001c0002t0002g0038 a0001c0002t0002g0064 a0001c0002t0002g0077 others(4): Show |
7 | HG02602.hp2 HG02647.hp1 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+2243_185+2253d others(13): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44964298 | ||||||
| chr19:44964298 | CT | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(98): Show |
128 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.185+2253delT | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44964298 | ||||||
| chr19:44964298 | CTT | C | 10 | a0001c0001t0001g0255 a0001c0003t0001g0095 a0001c0003t0001g0100 others(7): Show |
10 | HG01074.hp1 HG01099.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.185+2252_185+2253d others(4): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44964298 | ||||||
| chr19:44964298 | CTTTTT | C | 6 | a0001c0001t0010g0040 a0001c0005t0001g0202 a0001c0006t0001g0029 others(3): Show |
6 | HG00738.hp2 HG02257.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+2249_185+2253d others(7): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44964298 | ||||||
| chr19:44964298 | CTTTTTTT others(5): Show |
C | 1 | a0001c0015t0001g0199 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.185+2242_185+2253d others(14): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44964298 | ||||||
| chr19:44964337 | G | T | 1 | a0001c0002t0002g0068 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.185+2262G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44964337 | |||||||
| chr19:44964370 | G | A | 4 | a0001c0006t0001g0029 a0001c0006t0001g0031 a0001c0006t0001g0032 others(1): Show |
4 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+2295G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44964370 | |||||||
| chr19:44964413 | C | T | 2 | a0001c0002t0001g0182 a0001c0002t0001g0183 |
2 | HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.185+2338C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44964413 | |||||||
| chr19:44964435 | T | G | 1 | a0001c0001t0001g0314 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.185+2360T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44964435 | |||||||
| chr19:44964441 | G | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(115): Show |
135 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.185+2366G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44964441 | |||||||
| chr19:44964531 | TAACTC | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(115): Show |
135 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.185+2457_185+2461d others(7): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44964531 | |||||||
| chr19:44964591 | G | A | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.185+2516G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44964591 | |||||||
| chr19:44964661 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.185+2586A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44964661 | |||||||
| chr19:44964881 | T | G | 1 | a0001c0001t0001g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.185+2806T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44964881 | |||||||
| chr19:44964955 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.185+2880C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44964955 | |||||||
| chr19:44964965 | A | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0254 |
2 | HG01109.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.185+2890A>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44964965 | |||||||
| chr19:44965076 | T | C | 1 | a0001c0012t0001g0118 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.185+3001T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44965076 | |||||||
| chr19:44965090 | AT | A | 9 | a0001c0005t0001g0033 a0001c0005t0001g0202 a0001c0005t0001g0203 others(6): Show |
9 | HG00738.hp2 HG01123.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.185+3025delT | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44965090 | ||||||
| chr19:44965186 | T | C | 3 | a0001c0001t0001g0042 a0001c0009t0001g0200 a0001c0009t0001g0201 |
3 | HG02109.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.185+3111T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44965186 | |||||||
| chr19:44965247 | C | G | 1 | a0001c0015t0001g0199 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.185+3172C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44965247 | |||||||
| chr19:44965388 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(160): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.185+3313C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44965388 | |||||||
| chr19:44965391 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.185+3316G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44965391 | |||||||
| chr19:44965586 | A | G | 10 | a0001c0005t0001g0033 a0001c0005t0001g0202 a0001c0005t0001g0203 others(7): Show |
10 | HG00738.hp2 HG01123.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.185+3511A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44965586 | |||||||
| chr19:44965643 | C | T | 1 | a0001c0003t0001g0123 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.185+3568C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44965643 | |||||||
| chr19:44965698 | C | T | 2 | a0001c0001t0006g0015 a0001c0001t0006g0041 |
3 | HG01243.hp2 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.185+3623C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44965698 | |||||||
| chr19:44965746 | G | A | 1 | a0001c0002t0002g0064 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.185+3671G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44965746 | |||||||
| chr19:44965766 | G | A | 1 | a0001c0018t0002g0071 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.185+3691G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44965766 | |||||||
| chr19:44965768 | G | C | 14 | a0001c0001t0001g0011 a0001c0001t0001g0206 a0001c0001t0001g0207 others(11): Show |
16 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.185+3693G>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44965768 | |||||||
| chr19:44965770 | T | C | 1 | a0001c0002t0001g0163 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.185+3695T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44965770 | |||||||
| chr19:44965812 | A | G | 1 | a0001c0002t0001g0136 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.185+3737A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44965812 | |||||||
| chr19:44965872 | A | G | 1 | a0001c0002t0001g0162 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.185+3797A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44965872 | |||||||
| chr19:44965945 | A | G | 1 | a0001c0009t0001g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.185+3870A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44965945 | |||||||
| chr19:44966100 | A | C | 10 | a0001c0005t0001g0033 a0001c0005t0001g0202 a0001c0005t0001g0203 others(7): Show |
10 | HG00738.hp2 HG01123.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.185+4025A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966100 | |||||||
| chr19:44966231 | G | A | 1 | a0001c0002t0001g0023 | 2 | NA18954.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.185+4156G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966231 | |||||||
| chr19:44966282 | G | A | 1 | a0001c0018t0002g0071 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.185+4207G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966282 | |||||||
| chr19:44966284 | G | A | 3 | a0001c0002t0001g0007 a0001c0002t0001g0027 a0001c0002t0001g0185 |
7 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+4209G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966284 | |||||||
| chr19:44966322 | G | A | 317 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(314): Show |
368 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.185+4247G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966322 | |||||||
| chr19:44966363 | A | G | 1 | a0001c0005t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.185+4288A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966363 | |||||||
| chr19:44966376 | A | C | 1 | a0001c0001t0001g0295 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.185+4301A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966376 | |||||||
| chr19:44966419 | A | AAAAT | 196 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(193): Show |
221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.185+4347_185+4348i others(6): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44966419 | ||||||
| chr19:44966486 | T | C | 2 | a0001c0007t0001g0131 a0001c0007t0001g0141 |
2 | NA18995.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.185+4411T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966486 | |||||||
| chr19:44966511 | G | A | 1 | a0001c0002t0001g0175 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.185+4436G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966511 | |||||||
| chr19:44966550 | G | A | 8 | a0001c0003t0001g0095 a0001c0003t0001g0100 a0001c0003t0001g0105 others(5): Show |
8 | HG01099.hp1 HG01109.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+4475G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966550 | |||||||
| chr19:44966557 | A | G | 3 | a0001c0005t0001g0203 a0001c0005t0001g0204 a0001c0005t0001g0205 |
3 | HG01123.hp2 HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.185+4482A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966557 | |||||||
| chr19:44966645 | C | T | 1 | a0001c0002t0001g0196 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.185+4570C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966645 | |||||||
| chr19:44966665 | C | T | 10 | a0001c0005t0001g0033 a0001c0005t0001g0202 a0001c0005t0001g0203 others(7): Show |
10 | HG00738.hp2 HG01123.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.185+4590C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966665 | |||||||
| chr19:44966770 | T | C | 1 | a0001c0002t0001g0183 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.185+4695T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966770 | |||||||
| chr19:44966831 | A | ATC | 4 | a0001c0001t0001g0042 a0001c0002t0001g0059 a0001c0009t0001g0200 others(1): Show |
4 | HG02109.hp1 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.185+4774_185+4775d others(4): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44966831 | ||||||
| chr19:44966935 | A | G | 45 | a0001c0001t0001g0276 a0001c0002t0002g0005 a0001c0002t0002g0018 others(42): Show |
50 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.185+4860A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966935 | |||||||
| chr19:44966966 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.185+4891C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966966 | |||||||
| chr19:44966991 | G | A | 1 | a0001c0003t0004g0102 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.185+4916G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966991 | |||||||
| chr19:44966996 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.185+4921A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966996 | |||||||
| chr19:44966997 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.185+4922G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966997 | |||||||
| chr19:44966998 | C | T | 20 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(17): Show |
23 | HG02015.hp2 HG02040.hp1 HG02080.hp1 others(20): Show |
intron_variant | MODIFIER | c.185+4923C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44966998 | |||||||
| chr19:44967032 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.185+4957A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44967032 | |||||||
| chr19:44967041 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(194): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.185+4966T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44967041 | |||||||
| chr19:44967042 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.185+4967C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44967042 | |||||||
| chr19:44967057 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.185+4982A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44967057 | |||||||
| chr19:44967068 | C | T | 4 | a0001c0006t0001g0029 a0001c0006t0001g0030 a0001c0006t0001g0031 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.185+4993C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44967068 | |||||||
| chr19:44967076 | C | T | 1 | a0001c0003t0001g0112 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.185+5001C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44967076 | |||||||
| chr19:44967087 | C | T | 84 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(81): Show |
101 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.185+5012C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44967087 | |||||||
| chr19:44967107 | C | T | 2 | a0001c0001t0001g0250 a0001c0001t0001g0305 |
2 | NA18961.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.185+5032C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44967107 | |||||||
| chr19:44967201 | G | C | 152 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(149): Show |
177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.185+5126G>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44967201 | |||||||
| chr19:44967234 | G | A | 2 | a0001c0002t0001g0132 a0001c0002t0001g0164 |
2 | HG00639.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.185+5159G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44967234 | |||||||
| chr19:44967236 | T | A | 1 | a0001c0001t0001g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.185+5161T>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44967236 | |||||||
| chr19:44967300 | C | G | 66 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(63): Show |
74 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.185+5225C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44967300 | |||||||
| chr19:44967514 | G | C | 1 | a0001c0002t0001g0059 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.185+5439G>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44967514 | |||||||
| chr19:44967546 | A | G | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.185+5471A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44967546 | |||||||
| chr19:44967606 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.186-5481G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44967606 | |||||||
| chr19:44967655 | C | CT | 20 | a0001c0001t0001g0042 a0001c0001t0006g0015 a0001c0001t0006g0041 others(17): Show |
21 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.186-5432_186-5431i others(3): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44967655 | |||||||
| chr19:44967656 | C | T | 257 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(254): Show |
298 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.186-5431C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44967656 | |||||||
| chr19:44967657 | C | A | 20 | a0001c0001t0001g0042 a0001c0001t0006g0015 a0001c0001t0006g0041 others(17): Show |
21 | HG00140.hp2 HG00738.hp2 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.186-5430C>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44967657 | |||||||
| chr19:44967657 | CA | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(129): Show |
151 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.186-5415delA | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44967657 | ||||||
| chr19:44967927 | G | A | 1 | a0001c0015t0001g0199 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.186-5160G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44967927 | |||||||
| chr19:44968051 | A | G | 2 | a0001c0001t0006g0015 a0001c0001t0006g0041 |
3 | HG01243.hp2 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.186-5036A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44968051 | |||||||
| chr19:44968401 | G | A | 8 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0241 others(5): Show |
8 | HG00673.hp2 HG01993.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-4686G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44968401 | |||||||
| chr19:44968485 | A | G | 18 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
20 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.186-4602A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44968485 | |||||||
| chr19:44968587 | A | G | 1 | a0001c0006t0001g0034 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.186-4500A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44968587 | |||||||
| chr19:44968864 | C | G | 4 | a0001c0006t0001g0029 a0001c0006t0001g0031 a0001c0006t0001g0032 others(1): Show |
4 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.186-4223C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44968864 | |||||||
| chr19:44968919 | G | A | 1 | a0001c0005t0001g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.186-4168G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44968919 | |||||||
| chr19:44968999 | C | T | 1 | a0001c0002t0002g0083 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.186-4088C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44968999 | |||||||
| chr19:44969004 | T | A | 27 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(24): Show |
30 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.186-4083T>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44969004 | |||||||
| chr19:44969193 | C | T | 1 | a0001c0004t0001g0057 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.186-3894C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44969193 | |||||||
| chr19:44969194 | G | A | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.186-3893G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44969194 | |||||||
| chr19:44969316 | A | G | 1 | a0001c0002t0001g0023 | 2 | NA18954.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.186-3771A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44969316 | |||||||
| chr19:44969381 | G | T | 1 | a0001c0001t0001g0294 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.186-3706G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44969381 | |||||||
| chr19:44969392 | C | T | 27 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(24): Show |
30 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.186-3695C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44969392 | |||||||
| chr19:44969687 | C | CT | 44 | a0001c0002t0002g0005 a0001c0002t0002g0018 a0001c0002t0002g0019 others(41): Show |
49 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.186-3382dupT | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44969687 | ||||||
| chr19:44969687 | CT | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(123): Show |
145 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.186-3382delT | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44969687 | ||||||
| chr19:44969687 | CTT | C | 21 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(18): Show |
22 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.186-3383_186-3382d others(4): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44969687 | ||||||
| chr19:44969749 | A | G | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.186-3338A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44969749 | |||||||
| chr19:44969767 | G | A | 1 | a0001c0005t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.186-3320G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44969767 | |||||||
| chr19:44969810 | A | C | 281 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(278): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.186-3277A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44969810 | |||||||
| chr19:44969840 | A | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(115): Show |
135 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.186-3247A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44969840 | |||||||
| chr19:44969848 | CGGCTAAT others(1136): Show |
C | 28 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(25): Show |
31 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.186-3187_186-2045d others(2): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44969848 | ||||||
| chr19:44969944 | T | C | 1 | a0001c0002t0001g0150 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.186-3143T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44969944 | |||||||
| chr19:44969975 | C | T | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.186-3112C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44969975 | |||||||
| chr19:44970110 | G | T | 1 | a0001c0005t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.186-2977G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44970110 | |||||||
| chr19:44970181 | C | T | 1 | a0001c0001t0001g0002 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.186-2906C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44970181 | |||||||
| chr19:44970400 | A | AT | 117 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(114): Show |
134 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.186-2670dupT | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44970400 | ||||||
| chr19:44970400 | AT | A | 82 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(79): Show |
95 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.186-2670delT | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44970400 | ||||||
| chr19:44970403 | T | A | 1 | a0001c0003t0001g0122 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.186-2684T>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44970403 | |||||||
| chr19:44970455 | AGTGGCAT others(4): Show |
A | 127 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(124): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.186-2627_186-2617d others(13): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44970455 | ||||||
| chr19:44970687 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.186-2400G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44970687 | |||||||
| chr19:44970893 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.186-2194C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44970893 | |||||||
| chr19:44970908 | G | A | 1 | a0001c0002t0002g0077 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.186-2179G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44970908 | |||||||
| chr19:44971019 | T | C | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.186-2068T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44971019 | |||||||
| chr19:44971082 | C | T | 1 | a0001c0014t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.186-2005C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44971082 | |||||||
| chr19:44971307 | T | C | 1 | a0001c0005t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.186-1780T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44971307 | |||||||
| chr19:44971336 | AAAT | A | 23 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(20): Show |
26 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.186-1749_186-1747d others(5): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44971336 | ||||||
| chr19:44971342 | AT | A | 23 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(20): Show |
26 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.186-1743delT | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44971342 | ||||||
| chr19:44971423 | C | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(115): Show |
135 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.186-1664C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44971423 | |||||||
| chr19:44971579 | T | G | 1 | a0001c0001t0001g0220 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.186-1508T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44971579 | |||||||
| chr19:44971580 | T | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(115): Show |
135 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.186-1507T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44971580 | |||||||
| chr19:44971604 | G | A | 2 | a0001c0002t0001g0182 a0001c0002t0001g0183 |
2 | HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.186-1483G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44971604 | |||||||
| chr19:44971619 | C | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(115): Show |
135 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.186-1468C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44971619 | |||||||
| chr19:44971839 | A | G | 282 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(279): Show |
324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.186-1248A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44971839 | |||||||
| chr19:44971867 | C | CT | 73 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0044 others(70): Show |
80 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.186-1198dupT | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44971867 | ||||||
| chr19:44971867 | C | CTT | 180 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(177): Show |
214 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.186-1199_186-1198d others(4): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44971867 | ||||||
| chr19:44971867 | C | CTTT | 17 | a0001c0001t0001g0206 a0001c0001t0001g0222 a0001c0001t0001g0226 others(14): Show |
17 | HG00438.hp2 HG02080.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.186-1200_186-1198d others(5): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44971867 | ||||||
| chr19:44971867 | CT | C | 7 | a0001c0003t0001g0114 a0001c0003t0001g0115 a0001c0003t0004g0102 others(4): Show |
7 | HG01099.hp1 HG01123.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.186-1198delT | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 44971867 | ||||||
| chr19:44972018 | G | A | 1 | a0001c0001t0001g0249 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.186-1069G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972018 | |||||||
| chr19:44972071 | A | G | 1 | a0001c0006t0001g0032 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.186-1016A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972071 | |||||||
| chr19:44972091 | G | T | 20 | a0001c0002t0001g0023 a0001c0002t0001g0024 a0001c0002t0001g0025 others(17): Show |
23 | HG02015.hp2 HG02040.hp1 HG02080.hp1 others(20): Show |
intron_variant | MODIFIER | c.186-996G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972091 | |||||||
| chr19:44972278 | C | T | 4 | a0001c0005t0001g0202 a0001c0005t0001g0203 a0001c0005t0001g0204 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-809C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972278 | |||||||
| chr19:44972279 | G | A | 1 | a0001c0003t0004g0103 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.186-808G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972279 | |||||||
| chr19:44972282 | C | G | 5 | a0001c0006t0001g0029 a0001c0006t0001g0030 a0001c0006t0001g0031 others(2): Show |
5 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.186-805C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972282 | |||||||
| chr19:44972286 | T | C | 2 | a0001c0002t0002g0083 a0001c0002t0002g0087 |
2 | HG01069.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.186-801T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972286 | |||||||
| chr19:44972291 | A | T | 2 | a0001c0002t0002g0083 a0001c0002t0002g0087 |
2 | HG01069.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.186-796A>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972291 | |||||||
| chr19:44972296 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.186-791G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972296 | |||||||
| chr19:44972308 | C | T | 3 | a0001c0002t0001g0007 a0001c0002t0001g0027 a0001c0002t0001g0185 |
7 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.186-779C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972308 | |||||||
| chr19:44972396 | C | T | 1 | a0001c0002t0002g0081 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.186-691C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972396 | |||||||
| chr19:44972404 | T | C | 2 | a0001c0002t0001g0143 a0001c0002t0001g0144 |
2 | HG03831.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.186-683T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972404 | |||||||
| chr19:44972440 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.186-647A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972440 | |||||||
| chr19:44972443 | G | T | 82 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(79): Show |
99 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.186-644G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972443 | |||||||
| chr19:44972451 | A | G | 1 | a0001c0014t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.186-636A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972451 | |||||||
| chr19:44972456 | A | G | 173 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(170): Show |
196 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.186-631A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972456 | |||||||
| chr19:44972529 | A | G | 1 | a0001c0015t0001g0199 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.186-558A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972529 | |||||||
| chr19:44972550 | C | T | 4 | a0001c0005t0001g0202 a0001c0005t0001g0203 a0001c0005t0001g0204 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-537C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972550 | |||||||
| chr19:44972681 | T | C | 29 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(26): Show |
32 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.186-406T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972681 | |||||||
| chr19:44972829 | G | T | 1 | a0001c0002t0002g0064 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.186-258G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972829 | |||||||
| chr19:44972833 | G | A | 2 | a0001c0002t0001g0146 a0001c0002t0001g0190 |
2 | HG03239.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.186-254G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972833 | |||||||
| chr19:44972878 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.186-209C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972878 | |||||||
| chr19:44972891 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.186-196G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972891 | |||||||
| chr19:44972926 | A | C | 1 | a0001c0003t0001g0098 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.186-161A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44972926 | |||||||
| chr19:44973038 | C | T | 2 | a0001c0001t0006g0015 a0001c0001t0006g0041 |
3 | HG01243.hp2 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.186-49C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 2/13 | chr19 | 44973038 | |||||||
| chr19:44973247 | T | G | 48 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(45): Show |
54 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.309+37T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | chr19 | 44973247 | |||||||
| chr19:44973400 | C | G | 48 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(45): Show |
54 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.309+190C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | chr19 | 44973400 | |||||||
| chr19:44973621 | C | T | 1 | a0001c0015t0001g0199 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.309+411C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | chr19 | 44973621 | |||||||
| chr19:44973761 | G | GTTT | 6 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0001g0246 others(3): Show |
6 | HG02135.hp1 HG02976.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.309+569_309+571dup others(3): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 44973761 | ||||||
| chr19:44973761 | G | GTTTT | 32 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0044 others(29): Show |
37 | HG00280.hp1 HG00738.hp2 HG02015.hp2 others(34): Show |
intron_variant | MODIFIER | c.309+568_309+571dup others(4): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 44973761 | ||||||
| chr19:44973761 | G | GTTTTT | 12 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0231 others(9): Show |
13 | HG00597.hp1 HG00735.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.309+567_309+571dup others(5): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 44973761 | ||||||
| chr19:44973761 | G | GTTTTTT | 57 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(54): Show |
62 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.309+566_309+571dup others(6): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 44973761 | ||||||
| chr19:44973761 | G | GTTTTTTT | 12 | a0001c0001t0001g0042 a0001c0001t0001g0209 a0001c0001t0001g0212 others(9): Show |
12 | HG01361.hp1 HG01517.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.309+565_309+571dup others(7): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 44973761 | ||||||
| chr19:44973761 | G | GTTTTTTT others(6): Show |
3 | a0001c0005t0001g0203 a0001c0005t0001g0204 a0001c0005t0001g0205 |
3 | HG01123.hp2 HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.309+559_309+571dup others(13): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 44973761 | ||||||
| chr19:44973761 | G | GTTTTTTT others(7): Show |
1 | a0001c0005t0001g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.309+558_309+571dup others(14): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 44973761 | ||||||
| chr19:44973762 | T | TTTTTTTG others(12): Show |
1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.309+558_309+559ins others(19): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 44973762 | ||||||
| chr19:44973764 | T | TTTTTTTG | 10 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0297 others(7): Show |
10 | HG01257.hp1 HG02615.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.309+560_309+561ins others(7): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 44973764 | ||||||
| chr19:44973765 | T | G | 2 | a0001c0002t0001g0146 a0001c0002t0001g0190 |
2 | HG03239.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.309+555T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | chr19 | 44973765 | |||||||
| chr19:44973765 | T | TTTTTTG | 141 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(138): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.309+560_309+561ins others(6): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 44973765 | ||||||
| chr19:44973854 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(85): Show |
105 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.310-585C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | chr19 | 44973854 | |||||||
| chr19:44973888 | C | T | 1 | a0001c0005t0001g0204 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.310-551C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | chr19 | 44973888 | |||||||
| chr19:44973914 | C | T | 7 | a0001c0003t0001g0003 a0001c0003t0001g0022 a0001c0003t0001g0111 others(4): Show |
12 | HG01943.hp1 HG01978.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.310-525C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | chr19 | 44973914 | |||||||
| chr19:44973925 | A | T | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.310-514A>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | chr19 | 44973925 | |||||||
| chr19:44973974 | C | G | 123 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(120): Show |
134 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.310-465C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | chr19 | 44973974 | |||||||
| chr19:44974027 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.310-412G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | chr19 | 44974027 | |||||||
| chr19:44974124 | G | A | 74 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(71): Show |
79 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.310-315G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | chr19 | 44974124 | |||||||
| chr19:44974135 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.310-304C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | chr19 | 44974135 | |||||||
| chr19:44974171 | G | T | 1 | a0001c0005t0001g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.310-268G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | chr19 | 44974171 | |||||||
| chr19:44974193 | T | G | 5 | a0001c0006t0001g0029 a0001c0006t0001g0030 a0001c0006t0001g0031 others(2): Show |
5 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.310-246T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | chr19 | 44974193 | |||||||
| chr19:44974362 | G | A | 1 | a0001c0014t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.310-77G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 3/13 | chr19 | 44974362 | |||||||
| chr19:44974602 | G | A | 7 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0001g0297 others(4): Show |
7 | HG00673.hp1 NA18952.hp1 NA18975.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.468+5G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44974602 | |||||||
| chr19:44974612 | C | T | 1 | a0001c0002t0001g0154 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.468+15C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44974612 | |||||||
| chr19:44974643 | A | C | 7 | a0001c0001t0001g0004 a0001c0001t0001g0223 a0001c0001t0001g0235 others(4): Show |
11 | HG00621.hp1 HG02135.hp2 NA18948.hp2 others(8): Show |
intron_variant | MODIFIER | c.468+46A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44974643 | |||||||
| chr19:44974694 | T | C | 282 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(279): Show |
324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.468+97T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44974694 | |||||||
| chr19:44974826 | G | C | 5 | a0001c0006t0001g0029 a0001c0006t0001g0030 a0001c0006t0001g0031 others(2): Show |
5 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+229G>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44974826 | |||||||
| chr19:44974845 | A | T | 1 | a0001c0015t0001g0199 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.468+248A>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44974845 | |||||||
| chr19:44974955 | G | T | 1 | a0001c0002t0001g0159 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.468+358G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44974955 | |||||||
| chr19:44974960 | AAGTGCAG others(11): Show |
A | 1 | a0001c0004t0001g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.468+366_468+383del others(18): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 44974960 | ||||||
| chr19:44975001 | C | T | 3 | a0001c0002t0001g0007 a0001c0002t0001g0027 a0001c0002t0001g0185 |
7 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+404C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44975001 | |||||||
| chr19:44975028 | A | G | 5 | a0001c0004t0001g0017 a0001c0004t0001g0049 a0001c0004t0001g0056 others(2): Show |
6 | HG02109.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+431A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44975028 | |||||||
| chr19:44975057 | G | GAGAC | 282 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(279): Show |
324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.468+463_468+464ins others(4): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 44975057 | ||||||
| chr19:44975095 | A | G | 4 | a0001c0001t0001g0288 a0001c0001t0001g0290 a0001c0010t0001g0289 others(1): Show |
4 | HG01257.hp1 HG01258.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+498A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44975095 | |||||||
| chr19:44975120 | C | T | 3 | a0001c0002t0001g0157 a0001c0002t0001g0158 a0001c0002t0001g0171 |
3 | HG02015.hp2 HG02040.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.468+523C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44975120 | |||||||
| chr19:44975424 | G | A | 1 | a0001c0004t0001g0058 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.468+827G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44975424 | |||||||
| chr19:44975559 | T | G | 117 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(114): Show |
134 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.468+962T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44975559 | |||||||
| chr19:44975566 | G | T | 2 | a0001c0002t0001g0156 a0001c0005t0001g0033 |
2 | NA18993.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.468+969G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44975566 | |||||||
| chr19:44975567 | T | G | 1 | a0001c0002t0001g0156 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.468+970T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44975567 | |||||||
| chr19:44975568 | T | G | 1 | a0001c0005t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.468+971T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44975568 | |||||||
| chr19:44975573 | G | C | 1 | a0001c0014t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.468+976G>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44975573 | |||||||
| chr19:44975631 | C | G | 2 | a0001c0001t0006g0015 a0001c0001t0006g0041 |
3 | HG01243.hp2 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.468+1034C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44975631 | |||||||
| chr19:44975731 | T | A | 1 | a0001c0005t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.468+1134T>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44975731 | |||||||
| chr19:44975788 | T | G | 2 | a0001c0002t0001g0193 a0001c0002t0009g0195 |
2 | HG01943.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.468+1191T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44975788 | |||||||
| chr19:44975843 | C | T | 5 | a0001c0004t0001g0017 a0001c0004t0001g0049 a0001c0004t0001g0056 others(2): Show |
6 | HG02109.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+1246C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44975843 | |||||||
| chr19:44975976 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.469-1367C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44975976 | |||||||
| chr19:44976135 | A | G | 1 | a0001c0014t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.469-1208A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44976135 | |||||||
| chr19:44976194 | A | T | 70 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(67): Show |
78 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.469-1149A>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44976194 | |||||||
| chr19:44976270 | T | C | 1 | a0001c0002t0002g0063 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.469-1073T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44976270 | |||||||
| chr19:44976285 | G | A | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.469-1058G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44976285 | |||||||
| chr19:44976296 | G | C | 1 | a0001c0001t0001g0281 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.469-1047G>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44976296 | |||||||
| chr19:44976345 | C | T | 2 | a0001c0009t0001g0200 a0001c0009t0001g0201 |
2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.469-998C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44976345 | |||||||
| chr19:44976383 | G | C | 4 | a0001c0004t0001g0017 a0001c0004t0001g0056 a0001c0004t0001g0057 others(1): Show |
5 | HG02109.hp2 HG02451.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.469-960G>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44976383 | |||||||
| chr19:44976402 | C | T | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.469-941C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44976402 | |||||||
| chr19:44976432 | C | T | 1 | a0001c0005t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.469-911C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44976432 | |||||||
| chr19:44976483 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.469-860A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44976483 | |||||||
| chr19:44976561 | T | A | 1 | a0001c0002t0001g0156 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.469-782T>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44976561 | |||||||
| chr19:44976572 | C | A | 1 | a0001c0002t0001g0156 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.469-771C>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44976572 | |||||||
| chr19:44976630 | C | T | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.469-713C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44976630 | |||||||
| chr19:44976754 | C | T | 1 | a0001c0005t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.469-589C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44976754 | |||||||
| chr19:44976780 | A | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(115): Show |
135 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.469-563A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44976780 | |||||||
| chr19:44976869 | A | G | 4 | a0001c0005t0001g0202 a0001c0005t0001g0203 a0001c0005t0001g0204 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-474A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44976869 | |||||||
| chr19:44976917 | G | A | 29 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(26): Show |
32 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.469-426G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44976917 | |||||||
| chr19:44977079 | A | C | 1 | a0001c0004t0001g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.469-264A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44977079 | |||||||
| chr19:44977086 | C | T | 2 | a0001c0009t0001g0200 a0001c0009t0001g0201 |
2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.469-257C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44977086 | |||||||
| chr19:44977096 | G | A | 2 | a0001c0012t0001g0118 a0001c0012t0001g0119 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.469-247G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44977096 | |||||||
| chr19:44977133 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.469-210C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44977133 | |||||||
| chr19:44977292 | T | C | 1 | a0001c0014t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.469-51T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 4/13 | chr19 | 44977292 | |||||||
| chr19:44977468 | G | T | 1 | a0001c0005t0001g0033 | 1 | NA19043.hp1 | splice_region_variant&intron_variant | LOW | c.586+8G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44977468 | |||||||
| chr19:44977730 | G | A | 3 | a0001c0005t0001g0203 a0001c0005t0001g0204 a0001c0005t0001g0205 |
3 | HG01123.hp2 HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.586+270G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44977730 | |||||||
| chr19:44977746 | G | A | 1 | a0001c0001t0001g0279 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.586+286G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44977746 | |||||||
| chr19:44977747 | A | G | 1 | a0001c0001t0001g0279 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.586+287A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44977747 | |||||||
| chr19:44977804 | A | G | 5 | a0001c0006t0001g0029 a0001c0006t0001g0030 a0001c0006t0001g0031 others(2): Show |
5 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+344A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44977804 | |||||||
| chr19:44977842 | G | A | 1 | a0001c0004t0001g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.586+382G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44977842 | |||||||
| chr19:44978025 | G | C | 3 | a0001c0002t0002g0069 a0001c0002t0002g0072 a0001c0002t0002g0073 |
3 | HG01070.hp1 HG01071.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.586+565G>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44978025 | |||||||
| chr19:44978055 | A | G | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.586+595A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44978055 | |||||||
| chr19:44978165 | G | A | 1 | a0001c0005t0001g0202 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.586+705G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44978165 | |||||||
| chr19:44978173 | G | A | 1 | a0001c0003t0001g0100 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.586+713G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44978173 | |||||||
| chr19:44978178 | G | C | 2 | a0001c0001t0001g0259 a0001c0001t0001g0269 |
2 | HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.586+718G>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44978178 | |||||||
| chr19:44978232 | C | G | 1 | a0005c0022t0001g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.586+772C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44978232 | |||||||
| chr19:44978297 | T | C | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.586+837T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44978297 | |||||||
| chr19:44978399 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.586+939G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44978399 | |||||||
| chr19:44978409 | C | CA | 46 | a0001c0002t0001g0059 a0001c0002t0001g0153 a0001c0002t0001g0156 others(43): Show |
51 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.586+963dupA | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 44978409 | ||||||
| chr19:44978409 | C | CAA | 82 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(79): Show |
99 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.586+962_586+963dup others(2): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 44978409 | ||||||
| chr19:44978470 | T | C | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.586+1010T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44978470 | |||||||
| chr19:44978605 | C | G | 1 | a0001c0002t0001g0059 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.586+1145C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44978605 | |||||||
| chr19:44978627 | C | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(115): Show |
135 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.586+1167C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44978627 | |||||||
| chr19:44978728 | A | G | 28 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(25): Show |
31 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.586+1268A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44978728 | |||||||
| chr19:44978900 | C | T | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.586+1440C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44978900 | |||||||
| chr19:44978944 | A | G | 281 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(278): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.586+1484A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44978944 | |||||||
| chr19:44978981 | C | CT | 29 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0044 others(26): Show |
32 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.586+1538dupT | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 44978981 | ||||||
| chr19:44978981 | CT | C | 84 | a0001c0001t0001g0215 a0001c0001t0001g0260 a0001c0001t0001g0282 others(81): Show |
101 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.586+1538delT | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 44978981 | ||||||
| chr19:44979020 | G | A | 6 | a0001c0002t0001g0059 a0001c0006t0001g0029 a0001c0006t0001g0030 others(3): Show |
6 | HG00738.hp2 HG02559.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+1560G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44979020 | |||||||
| chr19:44979222 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.586+1762G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44979222 | |||||||
| chr19:44979313 | C | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(115): Show |
135 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.586+1853C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44979313 | |||||||
| chr19:44979335 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.586+1875G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44979335 | |||||||
| chr19:44979340 | A | C | 1 | a0001c0005t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.586+1880A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44979340 | |||||||
| chr19:44979358 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.586+1898T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44979358 | |||||||
| chr19:44979370 | T | A | 5 | a0001c0004t0001g0017 a0001c0004t0001g0049 a0001c0004t0001g0056 others(2): Show |
6 | HG02109.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+1910T>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44979370 | |||||||
| chr19:44979384 | C | T | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.586+1924C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44979384 | |||||||
| chr19:44979409 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.586+1949C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44979409 | |||||||
| chr19:44979627 | T | C | 84 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(81): Show |
101 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.586+2167T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44979627 | |||||||
| chr19:44979689 | TTCTGAGT others(18): Show |
T | 1 | a0001c0002t0002g0093 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.586+2231_586+2255d others(27): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 44979689 | ||||||
| chr19:44979708 | A | C | 281 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(278): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.586+2248A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44979708 | |||||||
| chr19:44979813 | T | C | 1 | a0001c0002t0002g0093 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.586+2353T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44979813 | |||||||
| chr19:44979826 | T | G | 1 | a0001c0002t0001g0143 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.586+2366T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44979826 | |||||||
| chr19:44980062 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.586+2602T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980062 | |||||||
| chr19:44980089 | A | G | 1 | a0001c0002t0002g0093 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.586+2629A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980089 | |||||||
| chr19:44980178 | C | G | 1 | a0001c0005t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.586+2718C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980178 | |||||||
| chr19:44980181 | A | C | 148 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(145): Show |
168 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.586+2721A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980181 | |||||||
| chr19:44980263 | C | T | 1 | a0001c0002t0001g0159 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.586+2803C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980263 | |||||||
| chr19:44980363 | G | T | 1 | a0001c0014t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.586+2903G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980363 | |||||||
| chr19:44980464 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.586+3004G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980464 | |||||||
| chr19:44980488 | G | A | 1 | a0001c0002t0001g0059 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.586+3028G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980488 | |||||||
| chr19:44980499 | A | C | 1 | a0001c0018t0002g0071 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.586+3039A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980499 | |||||||
| chr19:44980508 | CA | C | 171 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0044 others(168): Show |
198 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.586+3067delA | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 44980508 | ||||||
| chr19:44980508 | CAA | C | 8 | a0001c0001t0001g0043 a0001c0002t0001g0129 a0001c0002t0002g0035 others(5): Show |
8 | HG01123.hp2 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.586+3066_586+3067d others(4): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 44980508 | ||||||
| chr19:44980523 | A | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0287 a0001c0001t0001g0301 others(2): Show |
7 | HG00140.hp1 HG00738.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.586+3063A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980523 | |||||||
| chr19:44980547 | A | G | 5 | a0001c0004t0001g0017 a0001c0004t0001g0049 a0001c0004t0001g0056 others(2): Show |
6 | HG02109.hp2 HG02451.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.586+3087A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980547 | |||||||
| chr19:44980587 | G | A | 30 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(27): Show |
33 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.586+3127G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980587 | |||||||
| chr19:44980649 | A | G | 1 | a0001c0002t0002g0093 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.586+3189A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980649 | |||||||
| chr19:44980788 | ACAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0260 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.586+3329_586+3341d others(15): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980788 | |||||||
| chr19:44980799 | T | A | 1 | a0001c0005t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.586+3339T>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980799 | |||||||
| chr19:44980802 | T | A | 1 | a0001c0001t0001g0260 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.586+3342T>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980802 | |||||||
| chr19:44980843 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.586+3383A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980843 | |||||||
| chr19:44980849 | T | A | 1 | a0001c0001t0001g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.586+3389T>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980849 | |||||||
| chr19:44980862 | A | G | 282 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(279): Show |
324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.586+3402A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980862 | |||||||
| chr19:44980982 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.586+3522C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44980982 | |||||||
| chr19:44981007 | G | GT | 7 | a0001c0001t0001g0260 a0001c0001t0001g0272 a0001c0001t0001g0275 others(4): Show |
7 | HG00438.hp2 HG01175.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+3554dupT | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 44981007 | ||||||
| chr19:44981043 | G | A | 5 | a0001c0006t0001g0029 a0001c0006t0001g0030 a0001c0006t0001g0031 others(2): Show |
5 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+3583G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44981043 | |||||||
| chr19:44981107 | C | T | 2 | a0001c0002t0001g0127 a0001c0002t0001g0152 |
2 | HG02647.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.586+3647C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44981107 | |||||||
| chr19:44981152 | A | AT | 7 | a0001c0001t0001g0016 a0001c0001t0001g0045 a0001c0001t0001g0046 others(4): Show |
8 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.586+3701dupT | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 44981152 | ||||||
| chr19:44981223 | C | G | 1 | a0001c0001t0001g0051 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.586+3763C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44981223 | |||||||
| chr19:44981357 | T | G | 1 | a0001c0005t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.587-3861T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44981357 | |||||||
| chr19:44981383 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.587-3835C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44981383 | |||||||
| chr19:44981506 | G | A | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.587-3712G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44981506 | |||||||
| chr19:44981710 | C | T | 1 | a0001c0004t0001g0057 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.587-3508C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44981710 | |||||||
| chr19:44981743 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.587-3475C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44981743 | |||||||
| chr19:44981757 | A | G | 2 | a0002c0008t0002g0070 a0002c0008t0002g0075 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.587-3461A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44981757 | |||||||
| chr19:44981971 | C | G | 1 | a0001c0002t0001g0169 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.587-3247C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44981971 | |||||||
| chr19:44982113 | T | TTGAG | 28 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(25): Show |
31 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.587-3104_587-3101d others(6): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 44982113 | ||||||
| chr19:44982151 | C | A | 6 | a0001c0002t0002g0035 a0001c0002t0002g0036 a0001c0002t0002g0037 others(3): Show |
6 | NA18963.hp1 NA18994.hp1 NA18997.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-3067C>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44982151 | |||||||
| chr19:44982205 | C | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(115): Show |
135 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.587-3013C>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44982205 | |||||||
| chr19:44982208 | G | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(115): Show |
135 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.587-3010G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44982208 | |||||||
| chr19:44982234 | G | A | 28 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(25): Show |
31 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.587-2984G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44982234 | |||||||
| chr19:44982325 | G | A | 1 | a0001c0005t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.587-2893G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44982325 | |||||||
| chr19:44982346 | CA | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(118): Show |
138 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.587-2858delA | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 44982346 | ||||||
| chr19:44982369 | C | T | 12 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0044 others(9): Show |
13 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.587-2849C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44982369 | |||||||
| chr19:44982602 | C | T | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.587-2616C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44982602 | |||||||
| chr19:44982737 | C | T | 1 | a0001c0006t0001g0034 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.587-2481C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44982737 | |||||||
| chr19:44982891 | G | A | 28 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(25): Show |
31 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.587-2327G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44982891 | |||||||
| chr19:44983060 | C | CA | 51 | a0001c0001t0001g0240 a0001c0001t0001g0250 a0001c0001t0001g0309 others(48): Show |
56 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.587-2142dupA | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 44983060 | ||||||
| chr19:44983060 | CA | C | 7 | a0001c0001t0001g0212 a0001c0001t0001g0252 a0001c0001t0001g0287 others(4): Show |
7 | HG01081.hp1 NA18942.hp2 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-2142delA | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 44983060 | ||||||
| chr19:44983257 | C | G | 1 | a0001c0001t0001g0285 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.587-1961C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44983257 | |||||||
| chr19:44983430 | G | C | 13 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0044 others(10): Show |
14 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.587-1788G>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44983430 | |||||||
| chr19:44983439 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.587-1779T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44983439 | |||||||
| chr19:44983473 | C | T | 28 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(25): Show |
31 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.587-1745C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44983473 | |||||||
| chr19:44983509 | C | G | 1 | a0001c0002t0001g0059 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.587-1709C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44983509 | |||||||
| chr19:44983617 | C | CA | 16 | a0001c0001t0001g0042 a0001c0001t0001g0047 a0001c0001t0001g0051 others(13): Show |
16 | HG01099.hp1 HG01891.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.587-1573dupA | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 44983617 | ||||||
| chr19:44983617 | CA | C | 139 | a0001c0001t0001g0013 a0001c0001t0001g0207 a0001c0001t0001g0212 others(136): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.587-1573delA | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 44983617 | ||||||
| chr19:44983617 | CAA | C | 82 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(79): Show |
98 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.587-1574_587-1573d others(4): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 44983617 | ||||||
| chr19:44983617 | CAAA | C | 8 | a0001c0001t0001g0215 a0001c0001t0001g0217 a0001c0001t0001g0223 others(5): Show |
8 | HG01257.hp1 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.587-1575_587-1573d others(5): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 44983617 | ||||||
| chr19:44983637 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.587-1581A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44983637 | |||||||
| chr19:44983641 | A | G | 5 | a0001c0001t0001g0235 a0001c0004t0001g0056 a0001c0006t0001g0029 others(2): Show |
5 | HG00621.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.587-1577A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44983641 | |||||||
| chr19:44983690 | C | T | 28 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(25): Show |
31 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.587-1528C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44983690 | |||||||
| chr19:44983782 | G | A | 4 | a0001c0005t0001g0202 a0001c0005t0001g0203 a0001c0005t0001g0204 others(1): Show |
4 | HG01123.hp2 HG02055.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.587-1436G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44983782 | |||||||
| chr19:44983783 | A | G | 1 | a0001c0002t0001g0149 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.587-1435A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44983783 | |||||||
| chr19:44983921 | C | T | 124 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(121): Show |
146 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.587-1297C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44983921 | |||||||
| chr19:44983949 | G | A | 4 | a0001c0002t0001g0006 a0001c0002t0001g0166 a0001c0002t0001g0167 others(1): Show |
7 | HG02145.hp1 HG02622.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.587-1269G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44983949 | |||||||
| chr19:44983973 | C | A | 1 | a0001c0002t0001g0059 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.587-1245C>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44983973 | |||||||
| chr19:44984043 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.587-1175G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44984043 | |||||||
| chr19:44984163 | A | C | 28 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(25): Show |
31 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.587-1055A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44984163 | |||||||
| chr19:44984257 | T | C | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.587-961T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44984257 | |||||||
| chr19:44984262 | A | G | 315 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(312): Show |
366 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(363): Show |
intron_variant | MODIFIER | c.587-956A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44984262 | |||||||
| chr19:44984361 | T | G | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.587-857T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44984361 | |||||||
| chr19:44984376 | T | G | 1 | a0007c0021t0001g0286 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.587-842T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44984376 | |||||||
| chr19:44984413 | A | T | 28 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(25): Show |
31 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.587-805A>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44984413 | |||||||
| chr19:44984642 | C | T | 5 | a0001c0006t0001g0029 a0001c0006t0001g0030 a0001c0006t0001g0031 others(2): Show |
5 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.587-576C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44984642 | |||||||
| chr19:44984666 | T | G | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.587-552T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44984666 | |||||||
| chr19:44984695 | T | G | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.587-523T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44984695 | |||||||
| chr19:44984750 | G | A | 1 | a0001c0005t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.587-468G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44984750 | |||||||
| chr19:44984811 | C | G | 1 | a0001c0003t0004g0104 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.587-407C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44984811 | |||||||
| chr19:44984835 | C | T | 13 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0044 others(10): Show |
14 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.587-383C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44984835 | |||||||
| chr19:44984854 | T | G | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.587-364T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44984854 | |||||||
| chr19:44984862 | T | G | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.587-356T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44984862 | |||||||
| chr19:44984875 | C | G | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.587-343C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44984875 | |||||||
| chr19:44984875 | C | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(113): Show |
133 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.587-343C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44984875 | |||||||
| chr19:44984883 | T | G | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.587-335T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44984883 | |||||||
| chr19:44985068 | G | A | 1 | a0001c0005t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.587-150G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44985068 | |||||||
| chr19:44985176 | A | G | 282 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(279): Show |
324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.587-42A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44985176 | |||||||
| chr19:44985211 | A | C | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | splice_region_variant&intron_variant | LOW | c.587-7A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 5/13 | chr19 | 44985211 | |||||||
| chr19:44985309 | T | C | 282 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(279): Show |
324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
splice_region_variant&intron_variant | LOW | c.672+6T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 6/13 | chr19 | 44985309 | |||||||
| chr19:44985350 | T | A | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.672+47T>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 6/13 | chr19 | 44985350 | |||||||
| chr19:44985722 | C | T | 1 | a0001c0015t0001g0199 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.672+419C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 6/13 | chr19 | 44985722 | |||||||
| chr19:44985727 | A | G | 289 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(286): Show |
331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.672+424A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 6/13 | chr19 | 44985727 | |||||||
| chr19:44985741 | C | A | 1 | a0001c0015t0001g0199 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.672+438C>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 6/13 | chr19 | 44985741 | |||||||
| chr19:44985797 | G | T | 2 | a0001c0009t0001g0200 a0001c0009t0001g0201 |
2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.672+494G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 6/13 | chr19 | 44985797 | |||||||
| chr19:44985850 | G | A | 6 | a0001c0001t0001g0299 a0001c0006t0001g0029 a0001c0006t0001g0030 others(3): Show |
6 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.672+547G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 6/13 | chr19 | 44985850 | |||||||
| chr19:44985853 | C | G | 1 | a0001c0005t0001g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.672+550C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 6/13 | chr19 | 44985853 | |||||||
| chr19:44985860 | G | A | 1 | a0001c0014t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.672+557G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 6/13 | chr19 | 44985860 | |||||||
| chr19:44985951 | G | A | 1 | a0001c0002t0001g0138 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.673-504G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 6/13 | chr19 | 44985951 | |||||||
| chr19:44985976 | G | A | 1 | a0001c0002t0001g0129 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.673-479G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 6/13 | chr19 | 44985976 | |||||||
| chr19:44986071 | G | T | 3 | a0001c0003t0001g0021 a0001c0003t0001g0098 a0001c0003t0001g0099 |
4 | HG01891.hp2 HG02145.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-384G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 6/13 | chr19 | 44986071 | |||||||
| chr19:44986138 | G | A | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.673-317G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 6/13 | chr19 | 44986138 | |||||||
| chr19:44986401 | A | C | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.673-54A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 6/13 | chr19 | 44986401 | |||||||
| chr19:44986416 | C | T | 1 | a0001c0002t0001g0135 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.673-39C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 6/13 | chr19 | 44986416 | |||||||
| chr19:44986441 | C | T | 1 | a0001c0002t0002g0077 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.673-14C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 6/13 | chr19 | 44986441 | |||||||
| chr19:44986625 | T | G | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.793+50T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/13 | chr19 | 44986625 | |||||||
| chr19:44986692 | C | T | 27 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(24): Show |
30 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.793+117C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/13 | chr19 | 44986692 | |||||||
| chr19:44986807 | C | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(115): Show |
135 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.793+232C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/13 | chr19 | 44986807 | |||||||
| chr19:44986837 | T | G | 1 | a0006c0020t0001g0244 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.793+262T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/13 | chr19 | 44986837 | |||||||
| chr19:44986848 | TTGCCAGC others(6): Show |
T | 1 | a0001c0001t0001g0262 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.793+274_793+286del others(13): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/13 | chr19 | 44986848 | |||||||
| chr19:44986854 | G | GTATCA | 3 | a0001c0006t0001g0029 a0001c0006t0001g0030 a0001c0006t0001g0031 |
3 | HG02572.hp2 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.793+279_793+280ins others(5): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/13 | chr19 | 44986854 | |||||||
| chr19:44986856 | T | C | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.793+281T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/13 | chr19 | 44986856 | |||||||
| chr19:44986858 | T | A | 3 | a0001c0006t0001g0029 a0001c0006t0001g0030 a0001c0006t0001g0031 |
3 | HG02572.hp2 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.793+283T>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/13 | chr19 | 44986858 | |||||||
| chr19:44986859 | T | A | 3 | a0001c0006t0001g0029 a0001c0006t0001g0030 a0001c0006t0001g0031 |
3 | HG02572.hp2 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.793+284T>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/13 | chr19 | 44986859 | |||||||
| chr19:44986860 | G | GGCC | 3 | a0001c0006t0001g0029 a0001c0006t0001g0030 a0001c0006t0001g0031 |
3 | HG02572.hp2 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.793+285_793+286ins others(3): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/13 | chr19 | 44986860 | |||||||
| chr19:44986862 | A | C | 3 | a0001c0006t0001g0029 a0001c0006t0001g0030 a0001c0006t0001g0031 |
3 | HG02572.hp2 HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.793+287A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/13 | chr19 | 44986862 | |||||||
| chr19:44986874 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.793+299A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/13 | chr19 | 44986874 | |||||||
| chr19:44986934 | A | G | 148 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(145): Show |
168 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.794-245A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/13 | chr19 | 44986934 | |||||||
| chr19:44987027 | A | G | 278 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(275): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.794-152A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/13 | chr19 | 44987027 | |||||||
| chr19:44987123 | C | T | 3 | a0001c0001t0001g0042 a0001c0009t0001g0200 a0001c0009t0001g0201 |
3 | HG02109.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.794-56C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/13 | chr19 | 44987123 | |||||||
| chr19:44987129 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.794-50C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/13 | chr19 | 44987129 | |||||||
| chr19:44987170 | G | A | 18 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
20 | HG00280.hp1 HG00597.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.794-9G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 7/13 | chr19 | 44987170 | |||||||
| chr19:44987444 | C | T | 1 | a0001c0002t0001g0196 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1038+21C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 8/13 | chr19 | 44987444 | |||||||
| chr19:44987583 | G | A | 1 | a0001c0002t0002g0086 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1038+160G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 8/13 | chr19 | 44987583 | |||||||
| chr19:44987710 | A | C | 1 | a0001c0001t0001g0262 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1038+287A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 8/13 | chr19 | 44987710 | |||||||
| chr19:44987774 | C | T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0290 |
2 | HG01361.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1039-306C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 8/13 | chr19 | 44987774 | |||||||
| chr19:44987890 | C | A | 1 | a0001c0001t0001g0295 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1039-190C>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 8/13 | chr19 | 44987890 | |||||||
| chr19:44987916 | A | G | 129 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(126): Show |
151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1039-164A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 8/13 | chr19 | 44987916 | |||||||
| chr19:44987979 | A | T | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1039-101A>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 8/13 | chr19 | 44987979 | |||||||
| chr19:44988237 | T | C | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1132+64T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44988237 | |||||||
| chr19:44988264 | C | T | 1 | a0001c0014t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1132+91C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44988264 | |||||||
| chr19:44988313 | C | T | 1 | a0007c0021t0001g0286 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1132+140C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44988313 | |||||||
| chr19:44988314 | T | C | 1 | a0007c0021t0001g0286 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1132+141T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44988314 | |||||||
| chr19:44988364 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1132+191C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44988364 | |||||||
| chr19:44988412 | A | T | 1 | a0007c0021t0001g0286 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1132+239A>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44988412 | |||||||
| chr19:44988520 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1132+347C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44988520 | |||||||
| chr19:44988542 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1132+369G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44988542 | |||||||
| chr19:44988547 | C | T | 1 | a0007c0021t0001g0286 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1132+374C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44988547 | |||||||
| chr19:44988687 | G | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(275): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.1132+514G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44988687 | |||||||
| chr19:44988786 | C | T | 2 | a0001c0001t0001g0250 a0001c0001t0001g0305 |
2 | NA18961.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1132+613C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44988786 | |||||||
| chr19:44988852 | C | A | 1 | a0007c0021t0001g0286 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1132+679C>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44988852 | |||||||
| chr19:44988853 | G | A | 1 | a0001c0014t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1132+680G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44988853 | |||||||
| chr19:44988891 | T | G | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1132+718T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44988891 | |||||||
| chr19:44988902 | G | A | 11 | a0001c0002t0002g0019 a0001c0002t0002g0060 a0001c0002t0002g0061 others(8): Show |
12 | HG00621.hp2 HG02602.hp2 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.1132+729G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44988902 | |||||||
| chr19:44988919 | G | A | 1 | a0001c0002t0002g0078 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1132+746G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44988919 | |||||||
| chr19:44988934 | A | T | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1132+761A>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44988934 | |||||||
| chr19:44989053 | T | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(275): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.1132+880T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44989053 | |||||||
| chr19:44989131 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1132+958A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44989131 | |||||||
| chr19:44989227 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1132+1054G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44989227 | |||||||
| chr19:44989301 | G | A | 86 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(83): Show |
103 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1133-1094G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44989301 | |||||||
| chr19:44989417 | T | C | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1133-978T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44989417 | |||||||
| chr19:44989455 | C | A | 1 | a0009c0023t0001g0284 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1133-940C>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44989455 | |||||||
| chr19:44989495 | G | A | 1 | a0001c0002t0002g0037 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1133-900G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44989495 | |||||||
| chr19:44989551 | AGAGCTCT others(11): Show |
A | 1 | a0001c0002t0001g0059 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1133-812_1133-795d others(20): Show |
CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 44989551 | ||||||
| chr19:44989666 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1133-729C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44989666 | |||||||
| chr19:44989769 | T | C | 1 | a0001c0009t0001g0200 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1133-626T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44989769 | |||||||
| chr19:44989803 | T | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(146): Show |
169 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1133-592T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44989803 | |||||||
| chr19:44989804 | G | A | 2 | a0001c0001t0006g0015 a0001c0001t0006g0041 |
3 | HG01243.hp2 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1133-591G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44989804 | |||||||
| chr19:44989875 | T | G | 275 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(272): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1133-520T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44989875 | |||||||
| chr19:44989914 | G | A | 5 | a0001c0006t0001g0029 a0001c0006t0001g0030 a0001c0006t0001g0031 others(2): Show |
5 | HG00738.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1133-481G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44989914 | |||||||
| chr19:44990044 | T | A | 1 | a0001c0002t0001g0135 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1133-351T>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44990044 | |||||||
| chr19:44990095 | G | T | 1 | a0001c0001t0001g0295 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1133-300G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44990095 | |||||||
| chr19:44990191 | G | C | 2 | a0001c0002t0002g0061 a0001c0002t0002g0092 |
2 | NA18962.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.1133-204G>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44990191 | |||||||
| chr19:44990219 | G | T | 1 | a0001c0002t0001g0168 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1133-176G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44990219 | |||||||
| chr19:44990227 | A | T | 1 | a0007c0021t0001g0286 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1133-168A>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44990227 | |||||||
| chr19:44990254 | A | G | 1 | a0001c0014t0002g0062 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1133-141A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44990254 | |||||||
| chr19:44990377 | C | G | 111 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(108): Show |
131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1133-18C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44990377 | |||||||
| chr19:44990384 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1133-11C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 9/13 | chr19 | 44990384 | |||||||
| chr19:44990632 | G | A | 1 | a0006c0020t0001g0244 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1323+47G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 10/13 | chr19 | 44990632 | |||||||
| chr19:44990642 | T | C | 1 | a0001c0002t0001g0150 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1323+57T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 10/13 | chr19 | 44990642 | |||||||
| chr19:44990678 | T | G | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1323+93T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 10/13 | chr19 | 44990678 | |||||||
| chr19:44990758 | A | C | 1 | a0001c0002t0001g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1324-92A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 10/13 | chr19 | 44990758 | |||||||
| chr19:44990952 | G | A | 1 | a0001c0002t0002g0068 | 1 | NA20905.hp2 | splice_region_variant&intron_variant | LOW | c.1419+7G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 11/13 | chr19 | 44990952 | |||||||
| chr19:44990987 | G | T | 1 | a0006c0020t0001g0244 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1419+42G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 11/13 | chr19 | 44990987 | |||||||
| chr19:44990988 | T | A | 1 | a0006c0020t0001g0244 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1419+43T>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 11/13 | chr19 | 44990988 | |||||||
| chr19:44990989 | A | C | 1 | a0006c0020t0001g0244 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1419+44A>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 11/13 | chr19 | 44990989 | |||||||
| chr19:44991086 | C | A | 2 | a0001c0003t0001g0020 a0001c0003t0001g0105 |
3 | HG02818.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1419+141C>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 11/13 | chr19 | 44991086 | |||||||
| chr19:44991090 | T | G | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1419+145T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 11/13 | chr19 | 44991090 | |||||||
| chr19:44991093 | C | T | 1 | a0001c0002t0002g0082 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1420-145C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 11/13 | chr19 | 44991093 | |||||||
| chr19:44991099 | C | T | 1 | a0001c0009t0001g0201 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1420-139C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 11/13 | chr19 | 44991099 | |||||||
| chr19:44991105 | C | T | 2 | a0001c0005t0001g0203 a0001c0005t0001g0205 |
2 | HG01123.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1420-133C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 11/13 | chr19 | 44991105 | |||||||
| chr19:44991385 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1555+12G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 12/13 | chr19 | 44991385 | |||||||
| chr19:44991442 | G | A | 2 | a0001c0001t0001g0259 a0001c0001t0001g0269 |
2 | HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1555+69G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 12/13 | chr19 | 44991442 | |||||||
| chr19:44991611 | T | G | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1555+238T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 12/13 | chr19 | 44991611 | |||||||
| chr19:44991769 | G | T | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1555+396G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 12/13 | chr19 | 44991769 | |||||||
| chr19:44991770 | T | G | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1555+397T>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 12/13 | chr19 | 44991770 | |||||||
| chr19:44991797 | T | C | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | NA18951.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.1555+424T>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 12/13 | chr19 | 44991797 | |||||||
| chr19:44991920 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1556-313G>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 12/13 | chr19 | 44991920 | |||||||
| chr19:44992054 | C | T | 1 | a0001c0003t0004g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1556-179C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 12/13 | chr19 | 44992054 | |||||||
| chr19:44992088 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1556-145C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 12/13 | chr19 | 44992088 | |||||||
| chr19:44992142 | A | G | 1 | a0003c0016t0008g0313 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1556-91A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 12/13 | chr19 | 44992142 | |||||||
| chr19:44992410 | G | C | 118 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(115): Show |
135 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.1723+10G>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 13/13 | chr19 | 44992410 | |||||||
| chr19:44992424 | A | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(146): Show |
169 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1723+24A>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 13/13 | chr19 | 44992424 | |||||||
| chr19:44992475 | G | T | 1 | a0001c0001t0010g0040 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1723+75G>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 13/13 | chr19 | 44992475 | |||||||
| chr19:44992484 | C | T | 1 | a0001c0002t0001g0191 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1723+84C>T | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 13/13 | chr19 | 44992484 | |||||||
| chr19:44992521 | C | G | 1 | a0009c0023t0001g0284 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1724-90C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 13/13 | chr19 | 44992521 | |||||||
| chr19:44992525 | G | C | 1 | a0009c0023t0001g0284 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1724-86G>C | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 13/13 | chr19 | 44992525 | |||||||
| chr19:44992526 | C | G | 1 | a0009c0023t0001g0284 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1724-85C>G | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 13/13 | chr19 | 44992526 | |||||||
| chr19:44992545 | C | A | 1 | a0001c0001t0001g0280 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1724-66C>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 13/13 | chr19 | 44992545 | |||||||
| chr19:44992556 | C | A | 1 | a0006c0020t0001g0244 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1724-55C>A | CLPTM1 | ENSG00000104853.16 | transcript | ENST00000337392.10 | protein_coding | 13/13 | chr19 | 44992556 |