Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1213 |
| ensemblid | ENSG00000141367.13 |
| hgncid | 2092 |
| symbol | CLTC |
| name | clathrin heavy chain |
| refseq_nuc | NM_004859.4 |
| refseq_prot | NP_004850.1 |
| ensembl_nuc | ENST00000269122.8 |
| ensembl_prot | ENSP00000269122.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 59619895 |
| end | 59696956 |
| strand | + |
| ver | v1.2 |
| region | chr17:59619895-59696956 |
| region5000 | chr17:59614895-59701956 |
| regionname0 | CLTC_chr17_59619895_59696956 |
| regionname5000 | CLTC_chr17_59614895_59701956 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1675 | 259 | 86 | 40 | 91 | 4 | 36 | 69 | CLTC_chr17_59614895_59701956 | CLTC | MAQIL others(1670): Show |
chr17 | 59614895 | 59701956 |
| a0002 | 0/0 | 1675 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | MAQIL others(1670): Show |
chr17 | 59614895 | 59701956 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 5025 | 254 | 86 | 35 | 91 | 4 | 36 | CLTC_chr17_59614895_59701956 | CLTC | ATGGC others(5020): Show |
chr17 | 59614895 | 59701956 | ||
| a0001c0002 | 0/0 | 5025 | 4 | 0 | 4 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | ATGGC others(5020): Show |
chr17 | 59614895 | 59701956 | ||
| a0001c0004 | 0/0 | 5025 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | ATGGC others(5020): Show |
chr17 | 59614895 | 59701956 | ||
| a0002c0003 | 0/0 | 5025 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | ATGGC others(5020): Show |
chr17 | 59614895 | 59701956 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 8372 | 103 | 28 | 19 | 37 | 2 | 16 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8367): Show |
chr17 | 59614895 | 59701956 |
| a0001c0001t0002 | 0/0 | 8368 | 66 | 3 | 3 | 43 | 1 | 16 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8363): Show |
chr17 | 59614895 | 59701956 |
| a0001c0001t0003 | 1/0 | 8369 | 27 | 9 | 8 | 6 | 1 | 2 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8364): Show |
chr17 | 59614895 | 59701956 |
| a0001c0001t0004 | 0/0 | 8372 | 17 | 16 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8367): Show |
chr17 | 59614895 | 59701956 |
| a0001c0001t0005 | 0/0 | 8375 | 11 | 9 | 1 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8370): Show |
chr17 | 59614895 | 59701956 |
| a0001c0001t0006 | 0/0 | 8372 | 9 | 9 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8367): Show |
chr17 | 59614895 | 59701956 |
| a0001c0001t0007 | 0/0 | 8372 | 8 | 8 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8367): Show |
chr17 | 59614895 | 59701956 |
| a0001c0001t0008 | 0/0 | 8369 | 3 | 3 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8364): Show |
chr17 | 59614895 | 59701956 |
| a0001c0001t0009 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | AGCAG others(8367): Show |
chr17 | 59614895 | 59701956 |
| a0001c0001t0010 | 0/0 | 8372 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8367): Show |
chr17 | 59614895 | 59701956 |
| a0001c0001t0011 | 0/0 | 8372 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8367): Show |
chr17 | 59614895 | 59701956 |
| a0001c0001t0012 | 0/0 | 8372 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8367): Show |
chr17 | 59614895 | 59701956 |
| a0001c0001t0013 | 0/0 | 8372 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8367): Show |
chr17 | 59614895 | 59701956 |
| a0001c0001t0014 | 0/0 | 8368 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8363): Show |
chr17 | 59614895 | 59701956 |
| a0001c0001t0015 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8367): Show |
chr17 | 59614895 | 59701956 |
| a0001c0001t0016 | 0/0 | 8368 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8363): Show |
chr17 | 59614895 | 59701956 |
| a0001c0001t0017 | 0/0 | 8372 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8367): Show |
chr17 | 59614895 | 59701956 |
| a0001c0001t0018 | 0/0 | 8368 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8363): Show |
chr17 | 59614895 | 59701956 |
| a0001c0002t0002 | 0/0 | 8368 | 4 | 0 | 4 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8363): Show |
chr17 | 59614895 | 59701956 |
| a0001c0004t0001 | 0/0 | 8372 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8367): Show |
chr17 | 59614895 | 59701956 |
| a0002c0003t0001 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | AGCCG others(8367): Show |
chr17 | 59614895 | 59701956 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0199 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0001 | 0/0 | 11 | 0 | 0 | 9 | 0 | 2 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0007g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0007g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0008g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0009g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0010g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0011g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0012g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0013g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0014g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0015g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0016g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0017g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0001t0018g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0002t0002g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0001c0004t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| a0002c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0035 | EUR | GBR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | CHS | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | CHS | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | CHS | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0043 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0127 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01169 | hp2 | a0001 | c0001 | t0013 | g0179 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0074 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01433 | hp1 | a0001 | c0004 | t0001 | g0190 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01981 | hp2 | a0001 | c0001 | t0018 | g0157 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02004 | hp1 | a0001 | c0001 | t0012 | g0220 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02155 | hp1 | a0001 | c0001 | t0014 | g0130 | EAS | CDX | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CDX | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0061 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0073 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0069 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0065 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0047 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0076 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0067 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0080 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02735 | hp2 | a0001 | c0001 | t0011 | g0227 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0052 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0062 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0072 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0066 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0055 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0075 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0057 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0058 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0056 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0070 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0027 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0016 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0042 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0044 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0050 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0078 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0064 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | STU | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | BEB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | BEB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | STU | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | STU | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | BEB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG04199 | hp1 | a0001 | c0001 | t0017 | g0086 | SAS | STU | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | STU | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | STU | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | STU | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | YRI | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | YRI | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | YRI | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18972 | hp2 | a0001 | c0001 | t0009 | g0208 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18978 | hp2 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19000 | hp1 | a0001 | c0001 | t0015 | g0183 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0229 | AFR | LWK | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0082 | AFR | LWK | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | LWK | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19056 | hp2 | a0002 | c0003 | t0001 | g0100 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19062 | hp2 | a0001 | c0001 | t0016 | g0155 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0053 | AFR | YRI | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | YRI | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ASW | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | ASW | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0145 | EUR | TSI | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | TSI | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | GIH | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | GIH | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0083 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0084 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0003 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0051 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0059 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | USA | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0071 | AFR | USA | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0060 | AFR | USA | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | USA | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0081 | AFR | LWK | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| NA21309 | hp2 | a0001 | c0001 | t0007 | g0054 | AFR | LWK | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0199 | REF | REF | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0038 | REF | REF | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:59674745 | T | A | 1 | a0002 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.2463T>A | p.Asp821Glu | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/32 | 2700/8369 | 2463/5028 | 821/1675 | chr17 | 59674745 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:59644320 | C | T | 1 | a0001c0002 | 4 | HG01123.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
synonymous_variant | LOW | c.87C>T | p.Thr29Thr | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/32 | 324/8369 | 87/5028 | 29/1675 | chr17 | 59644320 | |||
| chr17:59681658 | G | A | 1 | a0001c0004 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.3261G>A | p.Glu1087Glu | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 21/32 | 3498/8369 | 3261/5028 | 1087/1675 | chr17 | 59681658 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:59619898 | C | A | 1 | a0001c0001t0009 | 1 | NA18972.hp2 | 5_prime_UTR_variant | MODIFIER | c.-234C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/32 | 234 | chr17 | 59619898 | ||||||
| chr17:59620006 | C | T | 1 | a0001c0001t0018 | 1 | HG01981.hp2 | 5_prime_UTR_variant | MODIFIER | c.-126C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/32 | 126 | chr17 | 59620006 | ||||||
| chr17:59620041 | C | A | 1 | a0001c0001t0010 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-91C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/32 | 91 | chr17 | 59620041 | ||||||
| chr17:59694430 | G | A | 1 | a0001c0001t0011 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*578G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 578 | chr17 | 59694430 | ||||||
| chr17:59694463 | A | G | 1 | a0001c0001t0017 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*611A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 611 | chr17 | 59694463 | ||||||
| chr17:59694538 | T | A | 1 | a0001c0001t0012 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*686T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 686 | chr17 | 59694538 | ||||||
| chr17:59695229 | A | G | 1 | a0001c0001t0016 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1377A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1377 | chr17 | 59695229 | ||||||
| chr17:59695452 | T | C | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1600T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1600 | chr17 | 59695452 | ||||||
| chr17:59695453 | C | T | 9 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0011 others(6): Show |
110 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1601C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1601 | chr17 | 59695453 | ||||||
| chr17:59695456 | G | T | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1604G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1604 | chr17 | 59695456 | ||||||
| chr17:59695470 | A | G | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1618A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1618 | chr17 | 59695470 | ||||||
| chr17:59695475 | G | T | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1623G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1623 | chr17 | 59695475 | ||||||
| chr17:59695482 | C | A | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1630C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1630 | chr17 | 59695482 | ||||||
| chr17:59695484 | T | G | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1632T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1632 | chr17 | 59695484 | ||||||
| chr17:59695486 | T | C | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1634T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1634 | chr17 | 59695486 | ||||||
| chr17:59695487 | C | T | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1635C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1635 | chr17 | 59695487 | ||||||
| chr17:59695488 | T | G | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1636T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1636 | chr17 | 59695488 | ||||||
| chr17:59695493 | A | C | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1641A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1641 | chr17 | 59695493 | ||||||
| chr17:59695552 | G | A | 1 | a0001c0001t0008 | 3 | HG01891.hp1 HG02559.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1700G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1700 | chr17 | 59695552 | ||||||
| chr17:59695672 | CAAAA | C | 5 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0016 others(2): Show |
73 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1824_*1827delAAAA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1824 | INFO_REALIGN_3_PRIME | chr17 | 59695672 | |||||
| chr17:59695735 | A | G | 1 | a0001c0001t0007 | 8 | HG02809.hp1 HG02896.hp1 HG03195.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1883A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1883 | chr17 | 59695735 | ||||||
| chr17:59695842 | AAAT | A | 18 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(15): Show |
218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*1998_*2000delATA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1998 | INFO_REALIGN_3_PRIME | chr17 | 59695842 | |||||
| chr17:59695850 | A | G | 1 | a0001c0001t0014 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1998A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1998 | chr17 | 59695850 | ||||||
| chr17:59696001 | T | C | 1 | a0001c0001t0015 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2149T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 2149 | chr17 | 59696001 | ||||||
| chr17:59696475 | G | A | 2 | a0001c0001t0006 a0001c0001t0007 |
17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2623G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 2623 | chr17 | 59696475 | ||||||
| chr17:59696525 | T | TAAAGAA | 19 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(16): Show |
229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*2676_*2677insGAAA others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 2677 | INFO_REALIGN_3_PRIME | chr17 | 59696525 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:59620477 | C | T | 1 | a0001c0001t0003g0015 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.42+304C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59620477 | |||||||
| chr17:59620785 | A | G | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG02055.hp1 HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.42+612A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59620785 | |||||||
| chr17:59620847 | C | G | 193 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(190): Show |
217 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.42+674C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59620847 | |||||||
| chr17:59621375 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.42+1202G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59621375 | |||||||
| chr17:59621459 | C | T | 10 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0043 others(7): Show |
10 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+1286C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59621459 | |||||||
| chr17:59621481 | G | T | 1 | a0001c0001t0007g0229 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.42+1308G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59621481 | |||||||
| chr17:59621659 | C | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(172): Show |
199 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.42+1486C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59621659 | |||||||
| chr17:59621853 | T | C | 1 | a0001c0001t0002g0068 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.42+1680T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59621853 | |||||||
| chr17:59621868 | C | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(54): Show |
64 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.42+1695C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59621868 | |||||||
| chr17:59621970 | G | A | 9 | a0001c0001t0006g0057 a0001c0001t0007g0051 a0001c0001t0007g0052 others(6): Show |
9 | HG02809.hp1 HG02896.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.42+1797G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59621970 | |||||||
| chr17:59622476 | C | A | 16 | a0001c0001t0004g0069 a0001c0001t0004g0070 a0001c0001t0004g0071 others(13): Show |
16 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.42+2303C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622476 | |||||||
| chr17:59622524 | T | C | 18 | a0001c0001t0004g0059 a0001c0001t0006g0057 a0001c0001t0006g0060 others(15): Show |
18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.42+2351T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622524 | |||||||
| chr17:59622627 | A | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
228 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.42+2454A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622627 | |||||||
| chr17:59622651 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0176 |
3 | HG00140.hp1 HG00544.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.42+2478G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622651 | |||||||
| chr17:59622696 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.42+2523A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622696 | |||||||
| chr17:59622735 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.42+2562A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622735 | |||||||
| chr17:59622876 | G | A | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0013g0179 |
3 | HG01099.hp1 HG01169.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.42+2703G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622876 | |||||||
| chr17:59622895 | T | C | 1 | a0001c0001t0010g0016 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.42+2722T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622895 | |||||||
| chr17:59622926 | G | A | 175 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(172): Show |
199 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.42+2753G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622926 | |||||||
| chr17:59622996 | A | G | 1 | a0001c0001t0007g0058 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.42+2823A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622996 | |||||||
| chr17:59623220 | G | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.42+3047G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59623220 | |||||||
| chr17:59623351 | T | G | 1 | a0001c0001t0001g0177 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.42+3178T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59623351 | |||||||
| chr17:59623530 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.42+3357G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59623530 | |||||||
| chr17:59623792 | C | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.42+3619C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59623792 | |||||||
| chr17:59623888 | C | T | 1 | a0001c0001t0011g0227 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.42+3715C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59623888 | |||||||
| chr17:59623945 | T | C | 6 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(3): Show |
6 | HG02698.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+3772T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59623945 | |||||||
| chr17:59624041 | C | T | 5 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0173 others(2): Show |
5 | HG00621.hp1 HG02015.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.42+3868C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59624041 | |||||||
| chr17:59624369 | A | G | 1 | a0001c0001t0002g0170 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.42+4196A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59624369 | |||||||
| chr17:59624454 | C | CT | 18 | a0001c0001t0001g0085 a0001c0001t0001g0120 a0001c0001t0002g0121 others(15): Show |
18 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.42+4306dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59624454 | ||||||
| chr17:59624454 | C | CTT | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
7 | HG01168.hp1 HG02109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+4305_42+4306dup others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59624454 | ||||||
| chr17:59624454 | C | CTTT | 29 | a0001c0001t0002g0008 a0001c0001t0002g0128 a0001c0001t0002g0129 others(26): Show |
32 | HG00639.hp1 HG00738.hp2 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.42+4304_42+4306dup others(3): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59624454 | ||||||
| chr17:59624454 | C | CTTTT | 23 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(20): Show |
35 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.42+4303_42+4306dup others(4): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59624454 | ||||||
| chr17:59624454 | CT | C | 89 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(86): Show |
97 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.42+4306delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59624454 | ||||||
| chr17:59624454 | CTTT | C | 14 | a0001c0001t0004g0059 a0001c0001t0006g0060 a0001c0001t0006g0061 others(11): Show |
14 | HG02257.hp1 HG02572.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+4304_42+4306del others(3): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59624454 | ||||||
| chr17:59624473 | T | G | 58 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(55): Show |
65 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.42+4300T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59624473 | |||||||
| chr17:59624567 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.42+4394C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59624567 | |||||||
| chr17:59624787 | A | T | 1 | a0001c0001t0002g0121 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.42+4614A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59624787 | |||||||
| chr17:59624789 | G | A | 1 | a0001c0001t0002g0121 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.42+4616G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59624789 | |||||||
| chr17:59624790 | T | G | 1 | a0001c0001t0002g0121 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.42+4617T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59624790 | |||||||
| chr17:59625110 | T | G | 1 | a0001c0001t0002g0128 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.42+4937T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625110 | |||||||
| chr17:59625213 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.42+5040A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625213 | |||||||
| chr17:59625231 | C | A | 1 | a0001c0001t0002g0121 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.42+5058C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625231 | |||||||
| chr17:59625254 | G | A | 1 | a0001c0001t0003g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.42+5081G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625254 | |||||||
| chr17:59625385 | G | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
228 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.42+5212G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625385 | |||||||
| chr17:59625481 | C | T | 1 | a0001c0001t0003g0039 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.42+5308C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625481 | |||||||
| chr17:59625492 | T | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
110 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.42+5319T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625492 | |||||||
| chr17:59625513 | A | G | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG02055.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.42+5340A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625513 | |||||||
| chr17:59625643 | C | T | 1 | a0001c0001t0006g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.42+5470C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625643 | |||||||
| chr17:59625781 | C | T | 4 | a0001c0001t0005g0048 a0001c0001t0005g0049 a0001c0001t0005g0050 others(1): Show |
4 | HG02896.hp2 HG03453.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+5608C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625781 | |||||||
| chr17:59625835 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.42+5662C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625835 | |||||||
| chr17:59625989 | A | C | 1 | a0001c0001t0001g0225 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.42+5816A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625989 | |||||||
| chr17:59625999 | A | T | 1 | a0001c0001t0001g0085 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.42+5826A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625999 | |||||||
| chr17:59626171 | A | G | 1 | a0001c0001t0011g0227 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.42+5998A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59626171 | |||||||
| chr17:59626314 | A | T | 1 | a0001c0001t0004g0083 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.42+6141A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59626314 | |||||||
| chr17:59626732 | G | A | 1 | a0001c0001t0003g0022 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.42+6559G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59626732 | |||||||
| chr17:59626907 | T | G | 1 | a0001c0001t0004g0059 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.42+6734T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59626907 | |||||||
| chr17:59626908 | G | C | 1 | a0001c0001t0001g0180 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.42+6735G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59626908 | |||||||
| chr17:59627073 | AT | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.42+6908delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59627073 | ||||||
| chr17:59627119 | T | C | 1 | a0001c0001t0003g0023 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.42+6946T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59627119 | |||||||
| chr17:59627123 | A | T | 1 | a0001c0001t0003g0005 | 2 | HG04184.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.42+6950A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59627123 | |||||||
| chr17:59627453 | C | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.42+7280C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59627453 | |||||||
| chr17:59627577 | T | C | 17 | a0001c0001t0006g0057 a0001c0001t0006g0060 a0001c0001t0006g0061 others(14): Show |
17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.42+7404T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59627577 | |||||||
| chr17:59627664 | A | C | 1 | a0001c0001t0001g0106 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.42+7491A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59627664 | |||||||
| chr17:59627991 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.42+7818A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59627991 | |||||||
| chr17:59628344 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.42+8171A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59628344 | |||||||
| chr17:59628510 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.42+8337A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59628510 | |||||||
| chr17:59628913 | C | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | NA19057.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.42+8740C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59628913 | |||||||
| chr17:59628942 | G | A | 1 | a0001c0001t0002g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.42+8769G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59628942 | |||||||
| chr17:59628960 | C | A | 1 | a0001c0001t0014g0130 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.42+8787C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59628960 | |||||||
| chr17:59629083 | CTT | C | 5 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0107 others(2): Show |
5 | HG02055.hp2 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+8912_42+8913del others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59629083 | ||||||
| chr17:59629518 | A | AT | 76 | a0001c0001t0001g0085 a0001c0001t0001g0095 a0001c0001t0001g0122 others(73): Show |
89 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.42+9365dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59629518 | ||||||
| chr17:59629518 | A | ATT | 108 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(105): Show |
118 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.42+9364_42+9365dup others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59629518 | ||||||
| chr17:59629518 | AT | A | 8 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(5): Show |
8 | HG01168.hp2 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.42+9365delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59629518 | ||||||
| chr17:59629899 | C | T | 1 | a0001c0001t0006g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.42+9726C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59629899 | |||||||
| chr17:59630092 | C | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.42+9919C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59630092 | |||||||
| chr17:59630151 | C | A | 1 | a0001c0001t0007g0051 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.42+9978C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59630151 | |||||||
| chr17:59630200 | C | T | 1 | a0001c0001t0012g0220 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.42+10027C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59630200 | |||||||
| chr17:59630392 | A | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.42+10219A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59630392 | |||||||
| chr17:59630568 | C | A | 17 | a0001c0001t0006g0057 a0001c0001t0006g0060 a0001c0001t0006g0061 others(14): Show |
17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.42+10395C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59630568 | |||||||
| chr17:59630582 | C | G | 3 | a0001c0001t0006g0064 a0001c0001t0006g0065 a0001c0001t0006g0066 |
3 | HG02572.hp1 HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.42+10409C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59630582 | |||||||
| chr17:59630826 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.42+10653A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59630826 | |||||||
| chr17:59630873 | G | A | 10 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0043 others(7): Show |
10 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+10700G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59630873 | |||||||
| chr17:59631237 | T | G | 2 | a0001c0001t0003g0020 a0001c0001t0003g0027 |
2 | HG02027.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.42+11064T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59631237 | |||||||
| chr17:59631384 | A | T | 18 | a0001c0001t0004g0059 a0001c0001t0006g0057 a0001c0001t0006g0060 others(15): Show |
18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.42+11211A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59631384 | |||||||
| chr17:59631450 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.42+11277A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59631450 | |||||||
| chr17:59631578 | T | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
228 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.42+11405T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59631578 | |||||||
| chr17:59631711 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.42+11538C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59631711 | |||||||
| chr17:59631778 | C | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0109 |
2 | HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.42+11605C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59631778 | |||||||
| chr17:59631969 | C | CA | 105 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(102): Show |
114 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.42+11812dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59631969 | ||||||
| chr17:59631969 | CA | C | 11 | a0001c0001t0002g0175 a0001c0001t0005g0041 a0001c0001t0005g0042 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.42+11812delA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59631969 | ||||||
| chr17:59632007 | C | A | 1 | a0001c0001t0003g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.42+11834C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632007 | |||||||
| chr17:59632087 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.42+11914G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632087 | |||||||
| chr17:59632158 | G | A | 17 | a0001c0001t0006g0057 a0001c0001t0006g0060 a0001c0001t0006g0061 others(14): Show |
17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.42+11985G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632158 | |||||||
| chr17:59632161 | G | A | 1 | a0001c0001t0006g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.42+11988G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632161 | |||||||
| chr17:59632224 | T | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(172): Show |
199 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.42+12051T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632224 | |||||||
| chr17:59632224 | T | G | 1 | a0001c0001t0002g0166 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.42+12051T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632224 | |||||||
| chr17:59632225 | G | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(86): Show |
97 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.43-12051G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632225 | |||||||
| chr17:59632346 | C | T | 1 | a0001c0001t0003g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.43-11930C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632346 | |||||||
| chr17:59632367 | C | CA | 166 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
190 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.43-11893dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59632367 | ||||||
| chr17:59632367 | C | CAA | 7 | a0001c0001t0001g0182 a0001c0001t0001g0184 a0001c0001t0001g0185 others(4): Show |
7 | HG01109.hp1 HG01433.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.43-11894_43-11893d others(4): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59632367 | ||||||
| chr17:59632453 | G | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.43-11823G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632453 | |||||||
| chr17:59632734 | C | G | 1 | a0001c0001t0003g0027 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.43-11542C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632734 | |||||||
| chr17:59633028 | TTGTCATT others(13): Show |
T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
110 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.43-11218_43-11199d others(22): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59633028 | ||||||
| chr17:59633258 | A | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-11018A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59633258 | |||||||
| chr17:59633319 | C | T | 1 | a0001c0001t0007g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.43-10957C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59633319 | |||||||
| chr17:59633398 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-10878C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59633398 | |||||||
| chr17:59633584 | C | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.43-10692C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59633584 | |||||||
| chr17:59633670 | TA | T | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.43-10604delA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59633670 | ||||||
| chr17:59634321 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG02055.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.43-9955C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59634321 | |||||||
| chr17:59634338 | G | T | 17 | a0001c0001t0006g0057 a0001c0001t0006g0060 a0001c0001t0006g0061 others(14): Show |
17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.43-9938G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59634338 | |||||||
| chr17:59634531 | G | T | 17 | a0001c0001t0006g0057 a0001c0001t0006g0060 a0001c0001t0006g0061 others(14): Show |
17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.43-9745G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59634531 | |||||||
| chr17:59634642 | C | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.43-9634C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59634642 | |||||||
| chr17:59634682 | CTA | C | 18 | a0001c0001t0004g0059 a0001c0001t0006g0057 a0001c0001t0006g0060 others(15): Show |
18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-9590_43-9589del others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59634682 | ||||||
| chr17:59634762 | A | G | 1 | a0001c0001t0003g0020 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.43-9514A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59634762 | |||||||
| chr17:59634828 | G | A | 1 | a0001c0001t0004g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.43-9448G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59634828 | |||||||
| chr17:59634966 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.43-9310G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59634966 | |||||||
| chr17:59635098 | GACCTATT others(83): Show |
G | 1 | a0001c0001t0004g0059 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.43-9177_43-9088del others(90): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59635098 | |||||||
| chr17:59635189 | G | C | 1 | a0001c0001t0004g0059 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.43-9087G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59635189 | |||||||
| chr17:59635488 | T | A | 3 | a0001c0001t0001g0182 a0001c0001t0001g0187 a0001c0001t0001g0218 |
3 | HG01261.hp2 HG02738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.43-8788T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59635488 | |||||||
| chr17:59635727 | A | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.43-8549A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59635727 | |||||||
| chr17:59635751 | A | G | 18 | a0001c0001t0004g0059 a0001c0001t0006g0057 a0001c0001t0006g0060 others(15): Show |
18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-8525A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59635751 | |||||||
| chr17:59635851 | G | A | 8 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0191 others(5): Show |
8 | HG01433.hp1 HG01978.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-8425G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59635851 | |||||||
| chr17:59635919 | A | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(94): Show |
106 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.43-8357A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59635919 | |||||||
| chr17:59636134 | C | CA | 10 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(7): Show |
10 | HG00408.hp1 HG01978.hp1 HG04199.hp1 others(7): Show |
intron_variant | MODIFIER | c.43-8128dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59636134 | ||||||
| chr17:59636159 | C | G | 1 | a0001c0001t0001g0217 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.43-8117C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59636159 | |||||||
| chr17:59636511 | G | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(86): Show |
97 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.43-7765G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59636511 | |||||||
| chr17:59636517 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.43-7759G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59636517 | |||||||
| chr17:59636788 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0194 a0001c0001t0001g0195 |
4 | HG00621.hp2 HG02040.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-7488G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59636788 | |||||||
| chr17:59636855 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-7421C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59636855 | |||||||
| chr17:59636932 | C | CT | 17 | a0001c0001t0001g0192 a0001c0001t0002g0128 a0001c0001t0002g0174 others(14): Show |
17 | HG00621.hp1 HG01891.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.43-7323dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59636932 | ||||||
| chr17:59636932 | CT | C | 40 | a0001c0001t0001g0006 a0001c0001t0001g0087 a0001c0001t0001g0088 others(37): Show |
41 | HG00738.hp1 HG01934.hp1 HG01978.hp1 others(38): Show |
intron_variant | MODIFIER | c.43-7323delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59636932 | ||||||
| chr17:59636970 | T | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.43-7306T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59636970 | |||||||
| chr17:59637361 | C | T | 2 | a0001c0002t0002g0004 a0001c0002t0002g0127 |
4 | HG01123.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-6915C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59637361 | |||||||
| chr17:59637389 | T | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.43-6887T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59637389 | |||||||
| chr17:59637554 | T | TA | 6 | a0001c0001t0001g0198 a0001c0001t0002g0121 a0001c0001t0002g0128 others(3): Show |
6 | HG02523.hp2 HG02738.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.43-6706dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59637554 | ||||||
| chr17:59637588 | T | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.43-6688T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59637588 | |||||||
| chr17:59637633 | T | C | 18 | a0001c0001t0004g0059 a0001c0001t0006g0057 a0001c0001t0006g0060 others(15): Show |
18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-6643T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59637633 | |||||||
| chr17:59637698 | C | CA | 20 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0028 others(17): Show |
20 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(17): Show |
intron_variant | MODIFIER | c.43-6560dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59637698 | ||||||
| chr17:59637698 | CA | C | 168 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
192 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.43-6560delA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59637698 | ||||||
| chr17:59637899 | G | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.43-6377G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59637899 | |||||||
| chr17:59637984 | CT | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-6289delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59637984 | ||||||
| chr17:59637986 | T | TA | 90 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(87): Show |
98 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.43-6290_43-6289ins others(1): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59637986 | |||||||
| chr17:59637987 | T | A | 207 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(204): Show |
232 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.43-6289T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59637987 | |||||||
| chr17:59638040 | A | T | 18 | a0001c0001t0004g0059 a0001c0001t0006g0057 a0001c0001t0006g0060 others(15): Show |
18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-6236A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59638040 | |||||||
| chr17:59638239 | G | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-6037G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59638239 | |||||||
| chr17:59638507 | TGGC | T | 214 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(211): Show |
240 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.43-5765_43-5763del others(3): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59638507 | ||||||
| chr17:59638550 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(86): Show |
97 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.43-5726C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59638550 | |||||||
| chr17:59638792 | C | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.43-5484C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59638792 | |||||||
| chr17:59638808 | G | A | 1 | a0001c0001t0004g0083 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.43-5468G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59638808 | |||||||
| chr17:59639349 | G | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.43-4927G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59639349 | |||||||
| chr17:59639803 | T | TA | 199 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(196): Show |
223 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.43-4458dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59639803 | ||||||
| chr17:59639822 | G | A | 1 | a0001c0001t0014g0130 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.43-4454G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59639822 | |||||||
| chr17:59639971 | A | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-4305A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59639971 | |||||||
| chr17:59640129 | A | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-4147A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59640129 | |||||||
| chr17:59640135 | A | G | 7 | a0001c0001t0007g0051 a0001c0001t0007g0052 a0001c0001t0007g0053 others(4): Show |
7 | HG02809.hp1 HG02896.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-4141A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59640135 | |||||||
| chr17:59640376 | C | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.43-3900C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59640376 | |||||||
| chr17:59640402 | C | CT | 33 | a0001c0001t0001g0007 a0001c0001t0001g0093 a0001c0001t0001g0094 others(30): Show |
34 | HG00639.hp2 HG01099.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.43-3860dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59640402 | ||||||
| chr17:59640550 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(86): Show |
97 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.43-3726C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59640550 | |||||||
| chr17:59640714 | T | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-3562T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59640714 | |||||||
| chr17:59640838 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.43-3438C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59640838 | |||||||
| chr17:59640916 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.43-3360C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59640916 | |||||||
| chr17:59641075 | TGCCACTG others(475): Show |
T | 1 | a0001c0001t0001g0012 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.43-3193_43-2712del | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641075 | ||||||
| chr17:59641117 | C | CA | 16 | a0001c0001t0002g0151 a0001c0001t0004g0069 a0001c0001t0004g0070 others(13): Show |
16 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.43-3148dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641117 | ||||||
| chr17:59641117 | C | CAA | 85 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(82): Show |
92 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.43-3149_43-3148dup others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641117 | ||||||
| chr17:59641398 | C | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-2878C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59641398 | |||||||
| chr17:59641475 | C | G | 18 | a0001c0001t0004g0059 a0001c0001t0006g0057 a0001c0001t0006g0060 others(15): Show |
18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-2801C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59641475 | |||||||
| chr17:59641603 | C | CA | 24 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(21): Show |
25 | HG01109.hp1 HG01255.hp2 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.43-2649dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641603 | ||||||
| chr17:59641603 | C | CAA | 88 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(85): Show |
96 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.43-2650_43-2649dup others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641603 | ||||||
| chr17:59641603 | C | CAAA | 48 | a0001c0001t0001g0112 a0001c0001t0001g0194 a0001c0001t0001g0219 others(45): Show |
63 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.43-2651_43-2649dup others(3): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641603 | ||||||
| chr17:59641603 | C | CAAAA | 16 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0232 others(13): Show |
16 | HG00423.hp2 HG02027.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.43-2652_43-2649dup others(4): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641603 | ||||||
| chr17:59641603 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.43-2659_43-2649del others(11): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641603 | ||||||
| chr17:59641943 | C | T | 1 | a0001c0001t0008g0003 | 3 | HG01891.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.43-2333C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59641943 | |||||||
| chr17:59641992 | C | T | 1 | a0001c0001t0006g0065 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.43-2284C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59641992 | |||||||
| chr17:59641999 | G | GT | 15 | a0001c0001t0001g0125 a0001c0001t0006g0057 a0001c0001t0006g0060 others(12): Show |
15 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.43-2253dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641999 | ||||||
| chr17:59641999 | GT | G | 29 | a0001c0001t0001g0224 a0001c0001t0002g0121 a0001c0001t0003g0015 others(26): Show |
32 | HG00140.hp2 HG01168.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.43-2253delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641999 | ||||||
| chr17:59641999 | GTTT | G | 8 | a0001c0001t0005g0042 a0001c0001t0005g0043 a0001c0001t0005g0044 others(5): Show |
8 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.43-2255_43-2253del others(3): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641999 | ||||||
| chr17:59642004 | T | TG | 11 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0102 others(8): Show |
12 | HG00738.hp2 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.43-2272_43-2271ins others(1): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642004 | |||||||
| chr17:59642005 | T | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(155): Show |
181 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.43-2271T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642005 | |||||||
| chr17:59642006 | T | G | 5 | a0001c0001t0001g0224 a0001c0001t0002g0121 a0001c0001t0004g0071 others(2): Show |
5 | HG03453.hp1 HG06807.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.43-2270T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642006 | |||||||
| chr17:59642011 | T | G | 2 | a0001c0001t0004g0077 a0001c0001t0004g0084 |
2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.43-2265T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642011 | |||||||
| chr17:59642012 | T | G | 1 | a0001c0001t0001g0228 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.43-2264T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642012 | |||||||
| chr17:59642013 | T | G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0099 |
2 | HG02723.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.43-2263T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642013 | |||||||
| chr17:59642207 | A | C | 18 | a0001c0001t0004g0059 a0001c0001t0006g0057 a0001c0001t0006g0060 others(15): Show |
18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-2069A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642207 | |||||||
| chr17:59642440 | G | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.43-1836G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642440 | |||||||
| chr17:59642441 | C | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.43-1835C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642441 | |||||||
| chr17:59642520 | A | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
228 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.43-1756A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642520 | |||||||
| chr17:59642702 | A | G | 1 | a0001c0001t0003g0024 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.43-1574A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642702 | |||||||
| chr17:59643099 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.43-1177G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59643099 | |||||||
| chr17:59643129 | T | TGG | 7 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0110 others(4): Show |
7 | HG02630.hp1 HG02698.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-1144_43-1143dup others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59643129 | ||||||
| chr17:59643132 | G | GGGGTGTG others(3): Show |
1 | a0001c0001t0002g0140 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.43-1143_43-1142ins others(10): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59643132 | ||||||
| chr17:59643132 | G | GGT | 8 | a0001c0001t0002g0008 a0001c0001t0002g0119 a0001c0001t0002g0156 others(5): Show |
11 | HG01891.hp1 HG02559.hp2 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.43-1109_43-1108dup others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59643132 | ||||||
| chr17:59643132 | G | GGTGT | 21 | a0001c0001t0002g0126 a0001c0001t0002g0141 a0001c0001t0003g0020 others(18): Show |
21 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.43-1111_43-1108dup others(4): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59643132 | ||||||
| chr17:59643132 | G | GGTGTGT | 55 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(52): Show |
70 | HG00423.hp2 HG00544.hp1 HG01123.hp1 others(67): Show |
intron_variant | MODIFIER | c.43-1113_43-1108dup others(6): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59643132 | ||||||
| chr17:59643132 | G | GGTGTGTG others(1): Show |
18 | a0001c0001t0002g0068 a0001c0001t0002g0135 a0001c0001t0002g0138 others(15): Show |
18 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-1115_43-1108dup others(8): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59643132 | ||||||
| chr17:59643132 | G | GGTGTGTG others(3): Show |
4 | a0001c0001t0002g0150 a0001c0001t0002g0165 a0001c0001t0005g0045 others(1): Show |
4 | HG00738.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-1117_43-1108dup others(10): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59643132 | ||||||
| chr17:59643132 | G | GGTGTGTG others(5): Show |
2 | a0001c0001t0005g0047 a0001c0001t0007g0056 |
2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.43-1119_43-1108dup others(12): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59643132 | ||||||
| chr17:59643132 | GGT | G | 16 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(13): Show |
17 | HG01099.hp2 HG01168.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.43-1109_43-1108del others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59643132 | ||||||
| chr17:59643134 | T | G | 63 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(60): Show |
70 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.43-1142T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59643134 | |||||||
| chr17:59643136 | T | G | 1 | a0001c0001t0001g0230 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.43-1140T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59643136 | |||||||
| chr17:59643138 | T | G | 1 | a0001c0001t0001g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.43-1138T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59643138 | |||||||
| chr17:59643380 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.43-896G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59643380 | |||||||
| chr17:59643516 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.43-760A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59643516 | |||||||
| chr17:59643780 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.43-496T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59643780 | |||||||
| chr17:59644175 | T | C | 4 | a0001c0001t0002g0126 a0001c0001t0002g0136 a0001c0001t0002g0138 others(1): Show |
4 | NA19057.hp1 NA19060.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-101T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59644175 | |||||||
| chr17:59644529 | G | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+46G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59644529 | |||||||
| chr17:59644535 | T | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.250+52T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59644535 | |||||||
| chr17:59644546 | T | G | 4 | a0001c0001t0001g0122 a0001c0001t0001g0125 a0001c0001t0001g0207 others(1): Show |
4 | HG02109.hp2 HG02280.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+63T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59644546 | |||||||
| chr17:59644546 | T | TTTTG | 170 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(167): Show |
194 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.250+79_250+82dupGT others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr17 | 59644546 | ||||||
| chr17:59644550 | G | T | 16 | a0001c0001t0006g0057 a0001c0001t0006g0060 a0001c0001t0006g0061 others(13): Show |
16 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.250+67G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59644550 | |||||||
| chr17:59644624 | C | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.250+141C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59644624 | |||||||
| chr17:59644641 | C | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.250+158C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59644641 | |||||||
| chr17:59645386 | G | C | 1 | a0001c0001t0002g0162 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.250+903G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59645386 | |||||||
| chr17:59645864 | C | CT | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.250+1383dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr17 | 59645864 | ||||||
| chr17:59645912 | G | A | 75 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(72): Show |
90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.250+1429G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59645912 | |||||||
| chr17:59645940 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.250+1457A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59645940 | |||||||
| chr17:59646514 | T | C | 1 | a0001c0001t0003g0030 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.251-884T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59646514 | |||||||
| chr17:59646548 | T | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-850T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59646548 | |||||||
| chr17:59646740 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.251-658C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59646740 | |||||||
| chr17:59646980 | C | A | 1 | a0001c0001t0002g0008 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.251-418C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59646980 | |||||||
| chr17:59647180 | A | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.251-218A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59647180 | |||||||
| chr17:59647222 | G | C | 1 | a0001c0001t0001g0212 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.251-176G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59647222 | |||||||
| chr17:59647682 | T | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
228 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.519+16T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 3/31 | chr17 | 59647682 | |||||||
| chr17:59647853 | C | T | 1 | a0001c0001t0016g0155 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.519+187C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 3/31 | chr17 | 59647853 | |||||||
| chr17:59648120 | G | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.520-120G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 3/31 | chr17 | 59648120 | |||||||
| chr17:59648923 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.681+522G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59648923 | |||||||
| chr17:59648994 | T | C | 17 | a0001c0001t0004g0069 a0001c0001t0004g0070 a0001c0001t0004g0071 others(14): Show |
17 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.681+593T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59648994 | |||||||
| chr17:59649330 | C | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.681+929C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59649330 | |||||||
| chr17:59649888 | G | GC | 204 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
228 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.682-1314dupC | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 59649888 | ||||||
| chr17:59649929 | A | G | 1 | a0001c0001t0004g0084 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.682-1274A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59649929 | |||||||
| chr17:59650275 | A | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.682-928A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59650275 | |||||||
| chr17:59650313 | T | A | 1 | a0001c0001t0001g0094 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.682-890T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59650313 | |||||||
| chr17:59650430 | C | T | 3 | a0001c0001t0002g0137 a0001c0001t0002g0147 a0001c0001t0002g0153 |
3 | NA18955.hp2 NA18972.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.682-773C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59650430 | |||||||
| chr17:59650483 | C | CT | 11 | a0001c0001t0001g0085 a0001c0001t0001g0124 a0001c0001t0001g0206 others(8): Show |
11 | HG00423.hp1 HG01243.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.682-698dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 59650483 | ||||||
| chr17:59650483 | CT | C | 58 | a0001c0001t0001g0225 a0001c0001t0002g0001 a0001c0001t0002g0008 others(55): Show |
73 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.682-698delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 59650483 | ||||||
| chr17:59650513 | A | G | 17 | a0001c0001t0006g0057 a0001c0001t0006g0060 a0001c0001t0006g0061 others(14): Show |
17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.682-690A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59650513 | |||||||
| chr17:59650555 | C | G | 1 | a0001c0001t0002g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.682-648C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59650555 | |||||||
| chr17:59650983 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(86): Show |
97 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.682-220C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59650983 | |||||||
| chr17:59651106 | A | G | 1 | a0001c0001t0003g0021 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.682-97A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59651106 | |||||||
| chr17:59651458 | A | G | 2 | a0001c0001t0001g0205 a0001c0001t0001g0219 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.795+142A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59651458 | |||||||
| chr17:59651654 | A | G | 2 | a0001c0001t0006g0062 a0001c0001t0006g0067 |
2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.795+338A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59651654 | |||||||
| chr17:59651655 | T | A | 1 | a0001c0001t0001g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.795+339T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59651655 | |||||||
| chr17:59651656 | A | G | 1 | a0001c0001t0008g0003 | 3 | HG01891.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.795+340A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59651656 | |||||||
| chr17:59651690 | A | C | 1 | a0001c0001t0001g0198 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.795+374A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59651690 | |||||||
| chr17:59652148 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.795+832G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59652148 | |||||||
| chr17:59652195 | G | A | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0226 |
3 | HG01109.hp1 HG01433.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.795+879G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59652195 | |||||||
| chr17:59652224 | T | C | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0013g0179 |
3 | HG01099.hp1 HG01169.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.795+908T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59652224 | |||||||
| chr17:59652483 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.795+1167T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59652483 | |||||||
| chr17:59652496 | C | T | 1 | a0001c0001t0003g0027 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.795+1180C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59652496 | |||||||
| chr17:59652588 | C | T | 3 | a0001c0001t0002g0137 a0001c0001t0002g0147 a0001c0001t0002g0153 |
3 | NA18955.hp2 NA18972.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.795+1272C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59652588 | |||||||
| chr17:59652678 | T | G | 17 | a0001c0001t0006g0057 a0001c0001t0006g0060 a0001c0001t0006g0061 others(14): Show |
17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.795+1362T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59652678 | |||||||
| chr17:59652828 | A | G | 102 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
111 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.795+1512A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59652828 | |||||||
| chr17:59652896 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.795+1580G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59652896 | |||||||
| chr17:59653070 | C | T | 1 | a0001c0001t0003g0035 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.795+1754C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59653070 | |||||||
| chr17:59653166 | T | C | 3 | a0001c0001t0006g0061 a0001c0001t0006g0062 a0001c0001t0006g0067 |
3 | HG02257.hp1 HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.795+1850T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59653166 | |||||||
| chr17:59653171 | GTTTA | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.795+1875_795+1878d others(6): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr17 | 59653171 | ||||||
| chr17:59653196 | A | T | 1 | a0001c0001t0002g0145 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.795+1880A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59653196 | |||||||
| chr17:59653204 | T | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(94): Show |
106 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.795+1888T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59653204 | |||||||
| chr17:59653256 | C | T | 10 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0043 others(7): Show |
10 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.795+1940C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59653256 | |||||||
| chr17:59653294 | C | T | 1 | a0001c0001t0007g0229 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.795+1978C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59653294 | |||||||
| chr17:59653444 | C | T | 75 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(72): Show |
90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.795+2128C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59653444 | |||||||
| chr17:59653852 | A | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.796-2002A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59653852 | |||||||
| chr17:59653961 | T | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.796-1893T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59653961 | |||||||
| chr17:59654206 | C | T | 10 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0043 others(7): Show |
10 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.796-1648C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59654206 | |||||||
| chr17:59654236 | C | T | 1 | a0001c0001t0007g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.796-1618C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59654236 | |||||||
| chr17:59654408 | CCTCAAGT others(296): Show |
C | 1 | a0001c0001t0001g0085 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.796-1441_796-1139d others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr17 | 59654408 | ||||||
| chr17:59654503 | C | T | 18 | a0001c0001t0004g0059 a0001c0001t0006g0057 a0001c0001t0006g0060 others(15): Show |
18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.796-1351C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59654503 | |||||||
| chr17:59654566 | C | T | 10 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(7): Show |
12 | HG01168.hp2 HG01891.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.796-1288C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59654566 | |||||||
| chr17:59654624 | T | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(188): Show |
215 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.796-1230T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59654624 | |||||||
| chr17:59654655 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.796-1199G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59654655 | |||||||
| chr17:59654732 | C | T | 3 | a0001c0001t0001g0182 a0001c0001t0001g0187 a0001c0001t0001g0218 |
3 | HG01261.hp2 HG02738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.796-1122C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59654732 | |||||||
| chr17:59654919 | A | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.796-935A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59654919 | |||||||
| chr17:59655224 | C | T | 75 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(72): Show |
90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.796-630C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59655224 | |||||||
| chr17:59655232 | G | T | 17 | a0001c0001t0004g0069 a0001c0001t0004g0070 a0001c0001t0004g0071 others(14): Show |
17 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.796-622G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59655232 | |||||||
| chr17:59655412 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.796-442G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59655412 | |||||||
| chr17:59655553 | G | A | 76 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(73): Show |
91 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.796-301G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59655553 | |||||||
| chr17:59655565 | C | CT | 75 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(72): Show |
90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.796-288dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr17 | 59655565 | ||||||
| chr17:59655596 | C | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.796-258C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59655596 | |||||||
| chr17:59655648 | T | C | 1 | a0001c0001t0002g0148 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.796-206T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59655648 | |||||||
| chr17:59656076 | T | C | 1 | a0001c0001t0005g0042 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.969+49T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656076 | |||||||
| chr17:59656118 | T | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
228 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.969+91T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656118 | |||||||
| chr17:59656262 | A | G | 1 | a0001c0001t0010g0016 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.969+235A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656262 | |||||||
| chr17:59656270 | A | T | 1 | a0001c0001t0003g0019 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.969+243A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656270 | |||||||
| chr17:59656399 | T | TC | 204 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
228 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.969+372_969+373ins others(1): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656399 | |||||||
| chr17:59656437 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
105 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.969+410A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656437 | |||||||
| chr17:59656545 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.969+518G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656545 | |||||||
| chr17:59656666 | A | AT | 15 | a0001c0001t0004g0069 a0001c0001t0004g0070 a0001c0001t0004g0074 others(12): Show |
15 | HG01243.hp2 HG01891.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.969+661dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr17 | 59656666 | ||||||
| chr17:59656666 | AT | A | 141 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(138): Show |
166 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.969+661delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr17 | 59656666 | ||||||
| chr17:59656670 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.969+643T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656670 | |||||||
| chr17:59656688 | T | C | 1 | a0001c0001t0003g0031 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.969+661T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656688 | |||||||
| chr17:59656705 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
110 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.969+678G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656705 | |||||||
| chr17:59656719 | G | A | 1 | a0001c0001t0004g0083 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.969+692G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656719 | |||||||
| chr17:59656963 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.969+936C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656963 | |||||||
| chr17:59657200 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.969+1173G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59657200 | |||||||
| chr17:59657203 | G | T | 3 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0025 |
3 | HG01168.hp2 HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.969+1176G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59657203 | |||||||
| chr17:59657299 | T | C | 214 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(211): Show |
240 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.969+1272T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59657299 | |||||||
| chr17:59657324 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.969+1297G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59657324 | |||||||
| chr17:59657329 | G | A | 75 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(72): Show |
90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.969+1302G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59657329 | |||||||
| chr17:59657678 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.969+1651G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59657678 | |||||||
| chr17:59657767 | C | CA | 5 | a0001c0001t0001g0096 a0001c0001t0001g0182 a0001c0001t0002g0142 others(2): Show |
5 | HG02602.hp2 HG02738.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.969+1757dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr17 | 59657767 | ||||||
| chr17:59657767 | CA | C | 5 | a0001c0001t0001g0110 a0001c0001t0001g0117 a0001c0001t0001g0224 others(2): Show |
5 | HG01099.hp2 HG02965.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.969+1757delA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr17 | 59657767 | ||||||
| chr17:59657798 | G | T | 1 | a0001c0001t0001g0203 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.969+1771G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59657798 | |||||||
| chr17:59657804 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.969+1777A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59657804 | |||||||
| chr17:59657974 | G | A | 1 | a0001c0001t0003g0032 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.969+1947G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59657974 | |||||||
| chr17:59658204 | A | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
110 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.969+2177A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59658204 | |||||||
| chr17:59658275 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.970-2116C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59658275 | |||||||
| chr17:59658323 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.970-2068C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59658323 | |||||||
| chr17:59658376 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.970-2015C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59658376 | |||||||
| chr17:59658624 | T | C | 2 | a0001c0001t0001g0205 a0001c0001t0001g0219 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.970-1767T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59658624 | |||||||
| chr17:59658965 | T | C | 214 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(211): Show |
240 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.970-1426T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59658965 | |||||||
| chr17:59658996 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.970-1395T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59658996 | |||||||
| chr17:59659304 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.970-1087A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59659304 | |||||||
| chr17:59659429 | ATTTTTAT | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.970-950_970-944del others(7): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr17 | 59659429 | ||||||
| chr17:59659453 | AT | A | 6 | a0001c0001t0001g0098 a0001c0001t0001g0125 a0001c0001t0001g0191 others(3): Show |
6 | HG00544.hp1 HG01978.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.970-923delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr17 | 59659453 | ||||||
| chr17:59659453 | ATT | A | 170 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(167): Show |
194 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.970-924_970-923del others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr17 | 59659453 | ||||||
| chr17:59659473 | CAG | C | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.970-915_970-914del others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr17 | 59659473 | ||||||
| chr17:59659619 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.970-772A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59659619 | |||||||
| chr17:59659649 | C | A | 1 | a0001c0001t0006g0063 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.970-742C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59659649 | |||||||
| chr17:59659762 | C | T | 1 | a0001c0001t0010g0016 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.970-629C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59659762 | |||||||
| chr17:59659877 | A | C | 1 | a0001c0001t0002g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.970-514A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59659877 | |||||||
| chr17:59660002 | A | C | 75 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(72): Show |
90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.970-389A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59660002 | |||||||
| chr17:59660136 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.970-255G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59660136 | |||||||
| chr17:59660627 | C | T | 10 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0043 others(7): Show |
10 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1167+39C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 7/31 | chr17 | 59660627 | |||||||
| chr17:59661066 | CTTAAT | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.1168-371_1168-367d others(7): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr17 | 59661066 | ||||||
| chr17:59661179 | AT | A | 18 | a0001c0001t0001g0085 a0001c0001t0006g0057 a0001c0001t0006g0060 others(15): Show |
18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.1168-251delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr17 | 59661179 | ||||||
| chr17:59661231 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1168-212A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 7/31 | chr17 | 59661231 | |||||||
| chr17:59661283 | C | T | 58 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(55): Show |
73 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1168-160C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 7/31 | chr17 | 59661283 | |||||||
| chr17:59661376 | C | G | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG02055.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1168-67C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 7/31 | chr17 | 59661376 | |||||||
| chr17:59661384 | G | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-59G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 7/31 | chr17 | 59661384 | |||||||
| chr17:59661712 | A | G | 1 | a0001c0001t0004g0081 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1368+69A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59661712 | |||||||
| chr17:59661906 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(86): Show |
97 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1368+263C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59661906 | |||||||
| chr17:59662018 | A | C | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1368+375A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59662018 | |||||||
| chr17:59662060 | A | G | 4 | a0001c0001t0002g0126 a0001c0001t0002g0136 a0001c0001t0002g0138 others(1): Show |
4 | NA19057.hp1 NA19060.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368+417A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59662060 | |||||||
| chr17:59662714 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
110 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1368+1071C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59662714 | |||||||
| chr17:59662831 | T | A | 17 | a0001c0001t0004g0069 a0001c0001t0004g0070 a0001c0001t0004g0071 others(14): Show |
17 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1369-1011T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59662831 | |||||||
| chr17:59662902 | T | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1369-940T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59662902 | |||||||
| chr17:59663161 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1369-681A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59663161 | |||||||
| chr17:59663393 | A | C | 1 | a0001c0001t0001g0210 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1369-449A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59663393 | |||||||
| chr17:59663558 | C | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0176 |
3 | HG00140.hp1 HG00544.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.1369-284C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59663558 | |||||||
| chr17:59663694 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1369-148A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59663694 | |||||||
| chr17:59664132 | T | A | 1 | a0001c0001t0007g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1521+138T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 9/31 | chr17 | 59664132 | |||||||
| chr17:59664425 | T | C | 58 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(55): Show |
73 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1522-362T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 9/31 | chr17 | 59664425 | |||||||
| chr17:59664450 | C | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.1522-337C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 9/31 | chr17 | 59664450 | |||||||
| chr17:59664550 | C | CA | 5 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0033 others(2): Show |
5 | HG01934.hp2 HG01952.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1522-220dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr17 | 59664550 | ||||||
| chr17:59664550 | CA | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(93): Show |
105 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1522-220delA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr17 | 59664550 | ||||||
| chr17:59664562 | AAAAAAG | A | 71 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(68): Show |
86 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1522-220_1522-215d others(8): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr17 | 59664562 | ||||||
| chr17:59664563 | AAAAAG | A | 5 | a0001c0001t0002g0128 a0001c0001t0002g0142 a0001c0001t0006g0064 others(2): Show |
5 | HG02572.hp1 HG02602.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1522-204_1522-200d others(7): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr17 | 59664563 | ||||||
| chr17:59665096 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1644+187A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 10/31 | chr17 | 59665096 | |||||||
| chr17:59665190 | A | T | 1 | a0001c0001t0004g0083 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1644+281A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 10/31 | chr17 | 59665190 | |||||||
| chr17:59665226 | GA | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.1644+329delA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 10/31 | INFO_REALIGN_3_PRIME | chr17 | 59665226 | ||||||
| chr17:59665249 | C | G | 1 | a0001c0001t0001g0201 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1644+340C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 10/31 | chr17 | 59665249 | |||||||
| chr17:59665335 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1644+426G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 10/31 | chr17 | 59665335 | |||||||
| chr17:59665475 | A | G | 58 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(55): Show |
73 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1644+566A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 10/31 | chr17 | 59665475 | |||||||
| chr17:59665766 | G | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1645-337G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 10/31 | chr17 | 59665766 | |||||||
| chr17:59666290 | T | C | 3 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0004t0001g0190 |
3 | HG01433.hp1 HG01978.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1782+50T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 11/31 | chr17 | 59666290 | |||||||
| chr17:59666330 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1782+90G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 11/31 | chr17 | 59666330 | |||||||
| chr17:59666372 | C | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1783-108C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 11/31 | chr17 | 59666372 | |||||||
| chr17:59666417 | G | A | 2 | a0001c0001t0002g0154 a0001c0001t0018g0157 |
2 | HG01981.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1783-63G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 11/31 | chr17 | 59666417 | |||||||
| chr17:59666455 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1783-25A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 11/31 | chr17 | 59666455 | |||||||
| chr17:59667051 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.2128+74G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59667051 | |||||||
| chr17:59667085 | A | C | 1 | a0001c0001t0003g0036 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2128+108A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59667085 | |||||||
| chr17:59667145 | T | G | 2 | a0001c0001t0005g0041 a0001c0001t0005g0046 |
2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2128+168T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59667145 | |||||||
| chr17:59667289 | A | G | 1 | a0001c0001t0003g0037 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2128+312A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59667289 | |||||||
| chr17:59667302 | G | A | 1 | a0001c0001t0004g0059 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2128+325G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59667302 | |||||||
| chr17:59667313 | C | T | 214 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(211): Show |
240 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.2128+336C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59667313 | |||||||
| chr17:59667409 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2128+432G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59667409 | |||||||
| chr17:59668196 | A | C | 1 | a0001c0001t0001g0225 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2129-581A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59668196 | |||||||
| chr17:59668288 | G | C | 1 | a0001c0001t0001g0210 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2129-489G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59668288 | |||||||
| chr17:59668511 | C | T | 16 | a0001c0001t0004g0069 a0001c0001t0004g0070 a0001c0001t0004g0071 others(13): Show |
16 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.2129-266C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59668511 | |||||||
| chr17:59668581 | G | T | 1 | a0001c0001t0002g0166 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2129-196G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59668581 | |||||||
| chr17:59668652 | C | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0214 |
2 | HG00639.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2129-125C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59668652 | |||||||
| chr17:59668746 | A | G | 75 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(72): Show |
90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.2129-31A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59668746 | |||||||
| chr17:59669692 | C | G | 6 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(3): Show |
6 | HG02698.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2292+752C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59669692 | |||||||
| chr17:59669724 | C | CTA | 80 | a0001c0001t0001g0085 a0001c0001t0001g0122 a0001c0001t0001g0123 others(77): Show |
95 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.2292+797_2292+798d others(4): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59669724 | ||||||
| chr17:59669737 | T | TATAA | 89 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(86): Show |
97 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.2292+798_2292+799i others(6): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59669737 | ||||||
| chr17:59669737 | T | TATATAA | 6 | a0001c0001t0001g0007 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
7 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.2292+798_2292+799i others(8): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59669737 | ||||||
| chr17:59669737 | T | TATATATA others(3): Show |
1 | a0001c0001t0001g0114 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2292+798_2292+799i others(12): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59669737 | ||||||
| chr17:59670059 | C | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0176 |
3 | HG00140.hp1 HG00544.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.2292+1119C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59670059 | |||||||
| chr17:59670178 | T | G | 58 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(55): Show |
73 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.2292+1238T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59670178 | |||||||
| chr17:59670223 | A | C | 5 | a0001c0001t0003g0005 a0001c0001t0003g0029 a0001c0001t0003g0030 others(2): Show |
6 | HG04184.hp2 NA18945.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.2292+1283A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59670223 | |||||||
| chr17:59670277 | GT | G | 153 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(150): Show |
176 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.2292+1348delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59670277 | ||||||
| chr17:59670282 | TTTTTTTG | T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0087 a0001c0001t0001g0088 others(18): Show |
22 | HG00738.hp1 HG01261.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.2292+1348_2292+135 others(11): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59670282 | ||||||
| chr17:59670295 | C | G | 22 | a0001c0001t0001g0006 a0001c0001t0001g0087 a0001c0001t0001g0088 others(19): Show |
23 | HG00738.hp1 HG01261.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.2292+1355C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59670295 | |||||||
| chr17:59670784 | C | T | 1 | a0001c0001t0006g0063 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2292+1844C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59670784 | |||||||
| chr17:59670926 | T | C | 1 | a0001c0001t0006g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2292+1986T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59670926 | |||||||
| chr17:59670964 | T | G | 3 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0017g0086 |
3 | HG02698.hp1 HG04199.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2292+2024T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59670964 | |||||||
| chr17:59671049 | C | T | 17 | a0001c0001t0006g0057 a0001c0001t0006g0060 a0001c0001t0006g0061 others(14): Show |
17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.2292+2109C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59671049 | |||||||
| chr17:59671158 | T | C | 1 | a0001c0001t0002g0009 | 2 | NA18964.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2292+2218T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59671158 | |||||||
| chr17:59671161 | A | G | 75 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(72): Show |
90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.2292+2221A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59671161 | |||||||
| chr17:59671226 | C | T | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.2292+2286C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59671226 | |||||||
| chr17:59671333 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.2293-2314G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59671333 | |||||||
| chr17:59671394 | A | C | 1 | a0001c0001t0003g0027 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2293-2253A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59671394 | |||||||
| chr17:59671795 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | NA19057.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2293-1852A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59671795 | |||||||
| chr17:59672450 | CTT | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.2293-1192_2293-119 others(6): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59672450 | ||||||
| chr17:59672488 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2293-1159C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59672488 | |||||||
| chr17:59672674 | T | A | 1 | a0001c0001t0001g0122 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2293-973T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59672674 | |||||||
| chr17:59673076 | G | GATATCTT others(6): Show |
1 | a0002c0003t0001g0100 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2293-569_2293-557d others(15): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59673076 | ||||||
| chr17:59673099 | GT | G | 173 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(170): Show |
197 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.2293-537delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59673099 | ||||||
| chr17:59673110 | T | C | 1 | a0001c0001t0005g0042 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2293-537T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59673110 | |||||||
| chr17:59673178 | A | T | 1 | a0002c0003t0001g0100 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2293-469A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59673178 | |||||||
| chr17:59673180 | T | A | 1 | a0002c0003t0001g0100 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2293-467T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59673180 | |||||||
| chr17:59673188 | T | C | 1 | a0001c0001t0006g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2293-459T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59673188 | |||||||
| chr17:59673439 | T | A | 1 | a0001c0001t0001g0205 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2293-208T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59673439 | |||||||
| chr17:59673514 | ATTCT | A | 2 | a0001c0001t0001g0188 a0001c0001t0015g0183 |
2 | NA18945.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.2293-126_2293-123d others(6): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59673514 | ||||||
| chr17:59673621 | T | C | 214 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(211): Show |
240 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.2293-26T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59673621 | |||||||
| chr17:59673843 | T | A | 1 | a0002c0003t0001g0100 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2418+71T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59673843 | |||||||
| chr17:59673860 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2418+88C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59673860 | |||||||
| chr17:59673861 | A | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.2418+89A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59673861 | |||||||
| chr17:59673930 | G | C | 1 | a0001c0001t0002g0128 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2418+158G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59673930 | |||||||
| chr17:59674062 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2418+290C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59674062 | |||||||
| chr17:59674093 | C | G | 1 | a0001c0001t0003g0028 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2418+321C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59674093 | |||||||
| chr17:59674101 | G | A | 1 | a0002c0003t0001g0100 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2418+329G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59674101 | |||||||
| chr17:59674103 | A | T | 1 | a0002c0003t0001g0100 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2418+331A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59674103 | |||||||
| chr17:59674104 | T | G | 1 | a0002c0003t0001g0100 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2418+332T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59674104 | |||||||
| chr17:59674132 | C | T | 10 | a0001c0001t0005g0041 a0001c0001t0005g0042 a0001c0001t0005g0043 others(7): Show |
10 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.2418+360C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59674132 | |||||||
| chr17:59674898 | A | G | 2 | a0001c0001t0001g0207 a0001c0001t0001g0214 |
2 | HG00639.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2561+55A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/31 | chr17 | 59674898 | |||||||
| chr17:59674910 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2561+67A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/31 | chr17 | 59674910 | |||||||
| chr17:59674935 | T | A | 1 | a0002c0003t0001g0100 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2561+92T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/31 | chr17 | 59674935 | |||||||
| chr17:59675107 | A | G | 1 | a0001c0001t0002g0166 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2561+264A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/31 | chr17 | 59675107 | |||||||
| chr17:59675126 | A | G | 9 | a0001c0001t0006g0057 a0001c0001t0007g0051 a0001c0001t0007g0052 others(6): Show |
9 | HG02809.hp1 HG02896.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.2561+283A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/31 | chr17 | 59675126 | |||||||
| chr17:59675417 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.2561+574G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/31 | chr17 | 59675417 | |||||||
| chr17:59675508 | C | T | 3 | a0001c0001t0001g0182 a0001c0001t0001g0187 a0001c0001t0001g0218 |
3 | HG01261.hp2 HG02738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2561+665C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/31 | chr17 | 59675508 | |||||||
| chr17:59675758 | A | G | 7 | a0001c0001t0001g0196 a0001c0001t0001g0200 a0001c0001t0001g0202 others(4): Show |
7 | HG02004.hp1 HG02135.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2561+915A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/31 | chr17 | 59675758 | |||||||
| chr17:59675915 | G | A | 1 | a0001c0001t0003g0033 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2562-1039G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/31 | chr17 | 59675915 | |||||||
| chr17:59677230 | A | G | 75 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(72): Show |
90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.2796+42A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59677230 | |||||||
| chr17:59677435 | T | TA | 8 | a0001c0001t0001g0006 a0001c0001t0001g0095 a0001c0001t0001g0096 others(5): Show |
9 | HG00738.hp1 HG01261.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.2796+248dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr17 | 59677435 | ||||||
| chr17:59677603 | G | C | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2796+415G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59677603 | |||||||
| chr17:59677833 | A | G | 1 | a0001c0001t0005g0050 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2796+645A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59677833 | |||||||
| chr17:59678049 | A | G | 1 | a0001c0001t0010g0016 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2796+861A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59678049 | |||||||
| chr17:59678219 | A | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.2796+1031A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59678219 | |||||||
| chr17:59678382 | C | CTT | 58 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(55): Show |
73 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.2797-1014_2797-101 others(6): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr17 | 59678382 | ||||||
| chr17:59678825 | C | T | 17 | a0001c0001t0006g0057 a0001c0001t0006g0060 a0001c0001t0006g0061 others(14): Show |
17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.2797-572C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59678825 | |||||||
| chr17:59678957 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
110 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.2797-440G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59678957 | |||||||
| chr17:59679129 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2797-268C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59679129 | |||||||
| chr17:59679165 | A | C | 1 | a0001c0001t0001g0090 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2797-232A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59679165 | |||||||
| chr17:59679290 | G | C | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | NA19057.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2797-107G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59679290 | |||||||
| chr17:59679388 | C | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797-9C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59679388 | |||||||
| chr17:59679939 | C | A | 1 | a0001c0001t0002g0149 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2919+420C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 18/31 | chr17 | 59679939 | |||||||
| chr17:59679962 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2919+443G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 18/31 | chr17 | 59679962 | |||||||
| chr17:59680003 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0217 |
2 | HG02155.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2919+484C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 18/31 | chr17 | 59680003 | |||||||
| chr17:59680328 | T | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(86): Show |
97 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.2920-584T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 18/31 | chr17 | 59680328 | |||||||
| chr17:59680563 | A | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.2920-349A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 18/31 | chr17 | 59680563 | |||||||
| chr17:59680719 | A | C | 75 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(72): Show |
90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.2920-193A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 18/31 | chr17 | 59680719 | |||||||
| chr17:59681149 | A | G | 1 | a0001c0001t0006g0057 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3065+92A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 19/31 | chr17 | 59681149 | |||||||
| chr17:59681185 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3066-110C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 19/31 | chr17 | 59681185 | |||||||
| chr17:59682061 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3443-210C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 21/31 | chr17 | 59682061 | |||||||
| chr17:59682591 | A | C | 1 | a0001c0001t0002g0142 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3601-38A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 22/31 | chr17 | 59682591 | |||||||
| chr17:59683018 | T | C | 18 | a0001c0001t0004g0059 a0001c0001t0006g0057 a0001c0001t0006g0060 others(15): Show |
18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
splice_region_variant&intron_variant | LOW | c.3873+4T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 24/31 | chr17 | 59683018 | |||||||
| chr17:59683089 | G | A | 2 | a0001c0001t0003g0026 a0001c0001t0003g0028 |
2 | HG03041.hp1 HG03225.hp1 |
splice_region_variant&intron_variant | LOW | c.3874-6G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 24/31 | chr17 | 59683089 | |||||||
| chr17:59683811 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4323+55G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 27/31 | chr17 | 59683811 | |||||||
| chr17:59684023 | CAT | C | 58 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(55): Show |
73 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.4434+40_4434+41del others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | INFO_REALIGN_3_PRIME | chr17 | 59684023 | ||||||
| chr17:59684257 | T | C | 1 | a0001c0001t0010g0016 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4434+272T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | chr17 | 59684257 | |||||||
| chr17:59684261 | T | C | 1 | a0001c0001t0004g0059 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4434+276T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | chr17 | 59684261 | |||||||
| chr17:59684361 | T | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4434+376T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | chr17 | 59684361 | |||||||
| chr17:59684662 | C | T | 57 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(54): Show |
72 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.4435-394C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | chr17 | 59684662 | |||||||
| chr17:59684672 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.4435-384G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | chr17 | 59684672 | |||||||
| chr17:59684801 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
110 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.4435-255C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | chr17 | 59684801 | |||||||
| chr17:59684806 | C | CAA | 16 | a0001c0001t0006g0057 a0001c0001t0006g0060 a0001c0001t0006g0061 others(13): Show |
16 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.4435-242_4435-241d others(4): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | INFO_REALIGN_3_PRIME | chr17 | 59684806 | ||||||
| chr17:59684806 | C | CAAA | 94 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
103 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.4435-243_4435-241d others(5): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | INFO_REALIGN_3_PRIME | chr17 | 59684806 | ||||||
| chr17:59684806 | C | CAAAA | 7 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(4): Show |
7 | HG01168.hp1 HG01243.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.4435-244_4435-241d others(6): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | INFO_REALIGN_3_PRIME | chr17 | 59684806 | ||||||
| chr17:59684806 | C | CAAAAA | 70 | a0001c0001t0001g0094 a0001c0001t0001g0215 a0001c0001t0002g0001 others(67): Show |
85 | HG00408.hp2 HG00423.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.4435-245_4435-241d others(7): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | INFO_REALIGN_3_PRIME | chr17 | 59684806 | ||||||
| chr17:59684806 | C | CAAAAAA | 6 | a0001c0001t0002g0128 a0001c0001t0002g0152 a0001c0001t0002g0159 others(3): Show |
6 | HG00544.hp1 HG00621.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.4435-246_4435-241d others(8): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | INFO_REALIGN_3_PRIME | chr17 | 59684806 | ||||||
| chr17:59684816 | G | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
228 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.4435-240G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | chr17 | 59684816 | |||||||
| chr17:59684858 | A | G | 1 | a0001c0001t0006g0063 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4435-198A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | chr17 | 59684858 | |||||||
| chr17:59685288 | TTATAATC | T | 2 | a0001c0001t0003g0026 a0001c0001t0003g0028 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4605+68_4605+74del others(7): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr17 | 59685288 | ||||||
| chr17:59685510 | T | C | 75 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(72): Show |
90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.4606-77T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 29/31 | chr17 | 59685510 | |||||||
| chr17:59685949 | T | A | 1 | a0001c0001t0005g0042 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4827+141T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59685949 | |||||||
| chr17:59686094 | T | G | 1 | a0001c0001t0004g0069 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4827+286T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59686094 | |||||||
| chr17:59686116 | G | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.4827+308G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59686116 | |||||||
| chr17:59686192 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.4827+384G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59686192 | |||||||
| chr17:59686332 | TATAAC | T | 56 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(53): Show |
71 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.4827+527_4827+531d others(7): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr17 | 59686332 | ||||||
| chr17:59686415 | C | G | 7 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.4827+607C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59686415 | |||||||
| chr17:59686632 | A | C | 1 | a0001c0001t0001g0215 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.4827+824A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59686632 | |||||||
| chr17:59686633 | C | A | 1 | a0001c0001t0001g0215 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.4827+825C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59686633 | |||||||
| chr17:59686648 | A | G | 1 | a0001c0001t0010g0016 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4827+840A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59686648 | |||||||
| chr17:59686769 | T | C | 1 | a0001c0001t0004g0078 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4827+961T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59686769 | |||||||
| chr17:59686817 | T | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.4827+1009T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59686817 | |||||||
| chr17:59687487 | G | GT | 16 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0001g0195 others(13): Show |
16 | HG01109.hp2 HG01243.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.4827+1692dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr17 | 59687487 | ||||||
| chr17:59687825 | C | T | 1 | a0001c0001t0008g0003 | 3 | HG01891.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4827+2017C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59687825 | |||||||
| chr17:59688241 | T | C | 1 | a0001c0001t0002g0138 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.4828-2395T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59688241 | |||||||
| chr17:59688347 | C | T | 204 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
228 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.4828-2289C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59688347 | |||||||
| chr17:59688646 | C | T | 1 | a0001c0001t0005g0046 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4828-1990C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59688646 | |||||||
| chr17:59689299 | C | T | 1 | a0001c0001t0010g0016 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4828-1337C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59689299 | |||||||
| chr17:59689384 | A | C | 18 | a0001c0001t0004g0059 a0001c0001t0006g0057 a0001c0001t0006g0060 others(15): Show |
18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.4828-1252A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59689384 | |||||||
| chr17:59689614 | T | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
111 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.4828-1022T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59689614 | |||||||
| chr17:59689924 | C | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(173): Show |
200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.4828-712C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59689924 | |||||||
| chr17:59690062 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4828-574A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59690062 | |||||||
| chr17:59690288 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4828-348C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59690288 | |||||||
| chr17:59690289 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.4828-347A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59690289 | |||||||
| chr17:59690322 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4828-314C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59690322 | |||||||
| chr17:59690348 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0125 |
2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4828-288G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59690348 | |||||||
| chr17:59690802 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4903+91A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59690802 | |||||||
| chr17:59691352 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4903+641C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59691352 | |||||||
| chr17:59691623 | T | TA | 15 | a0001c0001t0003g0039 a0001c0001t0004g0069 a0001c0001t0004g0070 others(12): Show |
15 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.4903+922dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 59691623 | ||||||
| chr17:59691623 | T | TAA | 51 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(48): Show |
66 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.4903+921_4903+922d others(4): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 59691623 | ||||||
| chr17:59691632 | A | AAT | 11 | a0001c0001t0001g0093 a0001c0001t0001g0123 a0001c0001t0001g0124 others(8): Show |
11 | HG01981.hp2 HG02027.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.4903+937_4903+938d others(4): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 59691632 | ||||||
| chr17:59691632 | A | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0089 a0001c0001t0001g0094 others(11): Show |
15 | HG00621.hp2 HG00639.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.4903+921A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59691632 | |||||||
| chr17:59691633 | AT | A | 1 | a0001c0001t0008g0003 | 3 | HG01891.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4903+923delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59691633 | |||||||
| chr17:59691634 | T | A | 26 | a0001c0001t0001g0006 a0001c0001t0001g0204 a0001c0001t0002g0137 others(23): Show |
26 | HG00423.hp2 HG01109.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.4903+923T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59691634 | |||||||
| chr17:59691636 | T | A | 1 | a0001c0001t0014g0130 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4903+925T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59691636 | |||||||
| chr17:59691837 | A | G | 77 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0002g0001 others(74): Show |
92 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.4903+1126A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59691837 | |||||||
| chr17:59692122 | T | G | 11 | a0001c0001t0004g0078 a0001c0001t0005g0041 a0001c0001t0005g0042 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.4903+1411T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692122 | |||||||
| chr17:59692171 | G | A | 2 | a0001c0002t0002g0004 a0001c0002t0002g0127 |
4 | HG01123.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.4903+1460G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692171 | |||||||
| chr17:59692292 | C | T | 1 | a0001c0001t0003g0034 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4904-1436C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692292 | |||||||
| chr17:59692307 | C | A | 14 | a0001c0001t0004g0059 a0001c0001t0006g0057 a0001c0001t0006g0061 others(11): Show |
14 | HG02257.hp1 HG02647.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.4904-1421C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692307 | |||||||
| chr17:59692308 | C | T | 4 | a0001c0001t0006g0060 a0001c0001t0006g0064 a0001c0001t0006g0065 others(1): Show |
4 | HG02572.hp1 HG02895.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.4904-1420C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692308 | |||||||
| chr17:59692323 | T | TAATAA | 204 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(201): Show |
228 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.4904-1403_4904-139 others(9): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 59692323 | ||||||
| chr17:59692328 | AACTGGTT others(3): Show |
A | 1 | a0001c0001t0013g0179 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4904-1398_4904-138 others(14): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 59692328 | ||||||
| chr17:59692346 | A | C | 1 | a0001c0001t0013g0179 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4904-1382A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692346 | |||||||
| chr17:59692348 | T | G | 1 | a0001c0001t0013g0179 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4904-1380T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692348 | |||||||
| chr17:59692349 | T | G | 1 | a0001c0001t0013g0179 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4904-1379T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692349 | |||||||
| chr17:59692350 | G | T | 1 | a0001c0001t0013g0179 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4904-1378G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692350 | |||||||
| chr17:59692637 | A | G | 76 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(73): Show |
83 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.4904-1091A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692637 | |||||||
| chr17:59692890 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4904-838G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692890 | |||||||
| chr17:59692927 | C | A | 2 | a0001c0001t0002g0163 a0001c0001t0002g0170 |
2 | HG02523.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.4904-801C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692927 | |||||||
| chr17:59693360 | CT | C | 41 | a0001c0001t0001g0007 a0001c0001t0001g0085 a0001c0001t0001g0114 others(38): Show |
42 | HG01099.hp2 HG01109.hp2 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.4904-348delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 59693360 | ||||||
| chr17:59693360 | CTT | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(133): Show |
159 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.4904-349_4904-348d others(4): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 59693360 | ||||||
| chr17:59693360 | CTTT | C | 9 | a0001c0001t0001g0089 a0001c0001t0001g0105 a0001c0001t0001g0181 others(6): Show |
9 | HG02280.hp1 HG02735.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.4904-350_4904-348d others(5): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 59693360 | ||||||
| chr17:59693381 | A | T | 2 | a0001c0001t0004g0059 a0001c0001t0010g0016 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4904-347A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59693381 | |||||||
| chr17:59693460 | A | G | 1 | a0001c0001t0006g0064 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4904-268A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59693460 | |||||||
| chr17:59693681 | C | T | 4 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0033 others(1): Show |
4 | HG01934.hp2 HG01952.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.4904-47C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59693681 |