Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1182 |
| ensemblid | ENSG00000109572.16 |
| hgncid | 2021 |
| symbol | CLCN3 |
| name | chloride voltage-gated channel 3 |
| refseq_nuc | NM_001829.4 |
| refseq_prot | NP_001820.2 |
| ensembl_nuc | ENST00000513761.6 |
| ensembl_prot | ENSP00000424603.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 169620578 |
| end | 169723673 |
| strand | + |
| ver | v1.2 |
| region | chr4:169620578-169723673 |
| region5000 | chr4:169615578-169728673 |
| regionname0 | CLCN3_chr4_169620578_169723673 |
| regionname5000 | CLCN3_chr4_169615578_169728673 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 818 | 287 | 95 | 50 | 88 | 16 | 36 | 62 | CLCN3_chr4_169615578_169728673 | CLCN3 | MESEQ others(813): Show |
chr4 | 169615578 | 169728673 |
| a0002 | 0/0 | 818 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | MESEQ others(813): Show |
chr4 | 169615578 | 169728673 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2454 | 167 | 54 | 32 | 44 | 9 | 26 | CLCN3_chr4_169615578_169728673 | CLCN3 | ATGGA others(2449): Show |
chr4 | 169615578 | 169728673 | ||
| a0001c0002 | 0/0 | 2454 | 66 | 10 | 12 | 35 | 4 | 5 | CLCN3_chr4_169615578_169728673 | CLCN3 | ATGGA others(2449): Show |
chr4 | 169615578 | 169728673 | ||
| a0001c0003 | 0/0 | 2454 | 50 | 29 | 5 | 8 | 3 | 5 | CLCN3_chr4_169615578_169728673 | CLCN3 | ATGGA others(2449): Show |
chr4 | 169615578 | 169728673 | ||
| a0001c0004 | 0/0 | 2454 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | ATGGA others(2449): Show |
chr4 | 169615578 | 169728673 | ||
| a0001c0006 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | ATGGA others(2449): Show |
chr4 | 169615578 | 169728673 | ||
| a0001c0007 | 0/0 | 2454 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | ATGGA others(2449): Show |
chr4 | 169615578 | 169728673 | ||
| a0001c0008 | 0/0 | 2454 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | ATGGA others(2449): Show |
chr4 | 169615578 | 169728673 | ||
| a0002c0005 | 0/0 | 2454 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | ATGGA others(2449): Show |
chr4 | 169615578 | 169728673 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6631 | 85 | 13 | 20 | 39 | 2 | 11 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6626): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0005 | 1/0 | 6635 | 13 | 11 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6630): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0006 | 0/0 | 6636 | 8 | 8 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6631): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0007 | 0/1 | 6651 | 8 | 2 | 1 | 0 | 3 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6646): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0010 | 0/0 | 6649 | 5 | 0 | 3 | 0 | 0 | 2 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6644): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0011 | 0/0 | 6624 | 4 | 4 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6619): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0012 | 0/0 | 6641 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6636): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0013 | 0/0 | 6645 | 4 | 0 | 1 | 1 | 1 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6640): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0014 | 0/0 | 6647 | 4 | 0 | 2 | 0 | 1 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6642): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0015 | 0/0 | 6632 | 3 | 3 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6627): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0016 | 0/0 | 6653 | 3 | 0 | 0 | 1 | 0 | 2 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6648): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0018 | 0/0 | 6631 | 2 | 0 | 1 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6626): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0019 | 0/0 | 6630 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6625): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0021 | 0/0 | 6633 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6628): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0024 | 0/0 | 6655 | 2 | 0 | 0 | 0 | 0 | 2 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6650): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0025 | 0/0 | 6636 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | GTCTT others(6631): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0026 | 0/0 | 6631 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6626): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0027 | 0/0 | 6648 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6643): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0028 | 0/0 | 6656 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6651): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0030 | 0/0 | 6631 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6626): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0031 | 0/0 | 6631 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6626): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0032 | 0/0 | 6631 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6626): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0033 | 0/0 | 6635 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6630): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0034 | 0/0 | 6635 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6630): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0035 | 0/0 | 6634 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6629): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0038 | 0/0 | 6637 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6632): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0042 | 0/0 | 6637 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6632): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0043 | 0/0 | 6638 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6633): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0044 | 0/0 | 6645 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6640): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0045 | 0/0 | 6647 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6642): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0047 | 0/0 | 6661 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6656): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0048 | 0/0 | 6663 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6658): Show |
chr4 | 169615578 | 169728673 |
| a0001c0001t0052 | 0/0 | 6650 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6645): Show |
chr4 | 169615578 | 169728673 |
| a0001c0002t0002 | 0/0 | 6635 | 48 | 0 | 7 | 33 | 3 | 5 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6630): Show |
chr4 | 169615578 | 169728673 |
| a0001c0002t0008 | 0/0 | 6633 | 6 | 4 | 1 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6628): Show |
chr4 | 169615578 | 169728673 |
| a0001c0002t0009 | 0/0 | 6632 | 5 | 5 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6627): Show |
chr4 | 169615578 | 169728673 |
| a0001c0002t0017 | 0/0 | 6635 | 3 | 0 | 2 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6630): Show |
chr4 | 169615578 | 169728673 |
| a0001c0002t0036 | 0/0 | 6635 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6630): Show |
chr4 | 169615578 | 169728673 |
| a0001c0002t0041 | 0/0 | 6637 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6632): Show |
chr4 | 169615578 | 169728673 |
| a0001c0002t0050 | 0/0 | 6635 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6630): Show |
chr4 | 169615578 | 169728673 |
| a0001c0002t0051 | 0/0 | 6633 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6628): Show |
chr4 | 169615578 | 169728673 |
| a0001c0003t0003 | 0/0 | 6634 | 24 | 8 | 2 | 7 | 3 | 4 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6629): Show |
chr4 | 169615578 | 169728673 |
| a0001c0003t0004 | 0/0 | 6634 | 15 | 13 | 2 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6629): Show |
chr4 | 169615578 | 169728673 |
| a0001c0003t0020 | 0/0 | 6634 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6629): Show |
chr4 | 169615578 | 169728673 |
| a0001c0003t0022 | 0/0 | 6636 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6631): Show |
chr4 | 169615578 | 169728673 |
| a0001c0003t0023 | 0/0 | 6636 | 2 | 1 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6631): Show |
chr4 | 169615578 | 169728673 |
| a0001c0003t0029 | 0/0 | 6620 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6615): Show |
chr4 | 169615578 | 169728673 |
| a0001c0003t0037 | 0/0 | 6638 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6633): Show |
chr4 | 169615578 | 169728673 |
| a0001c0003t0039 | 0/0 | 6636 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6631): Show |
chr4 | 169615578 | 169728673 |
| a0001c0003t0040 | 0/0 | 6637 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6632): Show |
chr4 | 169615578 | 169728673 |
| a0001c0003t0049 | 0/0 | 6634 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6629): Show |
chr4 | 169615578 | 169728673 |
| a0001c0004t0002 | 0/0 | 6635 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6630): Show |
chr4 | 169615578 | 169728673 |
| a0001c0006t0046 | 0/0 | 6655 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6650): Show |
chr4 | 169615578 | 169728673 |
| a0001c0007t0001 | 0/0 | 6631 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6626): Show |
chr4 | 169615578 | 169728673 |
| a0001c0008t0005 | 0/0 | 6635 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6630): Show |
chr4 | 169615578 | 169728673 |
| a0002c0005t0012 | 0/0 | 6641 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | CTCTT others(6636): Show |
chr4 | 169615578 | 169728673 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0005g0018 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0007g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0007g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0007g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0007g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0007g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0007g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0010g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0010g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0010g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0010g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0010g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0011g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0011g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0011g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0011g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0012g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0012g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0012g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0013g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0013g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0013g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0013g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0014g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0014g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0014g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0014g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0015g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0015g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0016g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0016g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0016g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0018g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0018g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0019g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0019g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0021g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0021g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0024g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0024g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0025g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0026g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0027g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0028g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0030g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0031g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0032g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0033g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0034g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0035g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0038g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0042g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0043g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0044g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0045g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0047g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0048g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0001t0052g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0008g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0008g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0009g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0009g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0017g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0017g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0036g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0041g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0050g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0002t0051g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0004g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0020g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0020g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0022g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0022g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0023g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0023g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0029g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0037g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0039g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0040g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0003t0049g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0004t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0006t0046g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0007t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0001c0008t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| a0002c0005t0012g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0007 | g0207 | EUR | GBR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00099 | hp2 | a0001 | c0001 | t0032 | g0181 | EUR | GBR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00140 | hp1 | a0001 | c0001 | t0007 | g0220 | EUR | GBR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0082 | EUR | GBR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0042 | EUR | FIN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | FIN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00323 | hp1 | a0001 | c0001 | t0018 | g0166 | EUR | FIN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00323 | hp2 | a0001 | c0001 | t0007 | g0209 | EUR | FIN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0092 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0095 | EAS | CHS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00639 | hp2 | a0001 | c0003 | t0004 | g0059 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00733 | hp1 | a0001 | c0007 | t0001 | g0158 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00733 | hp2 | a0001 | c0001 | t0007 | g0206 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00738 | hp1 | a0001 | c0001 | t0010 | g0228 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01069 | hp2 | a0001 | c0002 | t0050 | g0106 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01099 | hp1 | a0001 | c0001 | t0014 | g0221 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0065 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0241 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01109 | hp2 | a0001 | c0001 | t0028 | g0213 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01168 | hp2 | a0001 | c0001 | t0010 | g0230 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01175 | hp2 | a0001 | c0003 | t0004 | g0047 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0087 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01243 | hp1 | a0001 | c0001 | t0014 | g0224 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0084 | AMR | PUR | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01255 | hp1 | a0001 | c0001 | t0010 | g0208 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0062 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01257 | hp1 | a0001 | c0002 | t0017 | g0008 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01258 | hp1 | a0001 | c0001 | t0019 | g0013 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01258 | hp2 | a0001 | c0002 | t0017 | g0008 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01261 | hp1 | a0001 | c0001 | t0018 | g0168 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01261 | hp2 | a0001 | c0002 | t0041 | g0102 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01346 | hp1 | a0001 | c0003 | t0003 | g0030 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01358 | hp1 | a0001 | c0003 | t0023 | g0048 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01433 | hp2 | a0001 | c0001 | t0013 | g0225 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01496 | hp1 | a0001 | c0002 | t0008 | g0108 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01496 | hp2 | a0001 | c0001 | t0019 | g0126 | AMR | CLM | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01516 | hp1 | a0001 | c0002 | t0017 | g0150 | EUR | IBS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01516 | hp2 | a0001 | c0003 | t0003 | g0005 | EUR | IBS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01517 | hp1 | a0001 | c0003 | t0003 | g0005 | EUR | IBS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01517 | hp2 | a0001 | c0001 | t0014 | g0223 | EUR | IBS | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0190 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01884 | hp2 | a0001 | c0003 | t0029 | g0055 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0072 | AMR | PEL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01981 | hp1 | a0001 | c0003 | t0003 | g0037 | AMR | PEL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0086 | AMR | PEL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0109 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02040 | hp2 | a0001 | c0001 | t0016 | g0211 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02055 | hp1 | a0001 | c0008 | t0005 | g0235 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02055 | hp2 | a0001 | c0003 | t0003 | g0039 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02132 | hp2 | a0001 | c0003 | t0003 | g0029 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0083 | EAS | KHV | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02145 | hp2 | a0001 | c0003 | t0004 | g0058 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CDX | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02155 | hp2 | a0001 | c0002 | t0036 | g0097 | EAS | CDX | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0205 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02258 | hp2 | a0001 | c0001 | t0030 | g0237 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0085 | AMR | PEL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02280 | hp1 | a0001 | c0003 | t0040 | g0266 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02280 | hp2 | a0001 | c0003 | t0003 | g0032 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02451 | hp1 | a0001 | c0003 | t0004 | g0051 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02451 | hp2 | a0001 | c0002 | t0009 | g0061 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0186 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0191 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02602 | hp1 | a0001 | c0001 | t0016 | g0203 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02602 | hp2 | a0001 | c0001 | t0043 | g0248 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0193 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02615 | hp2 | a0001 | c0001 | t0015 | g0015 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0244 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02630 | hp1 | a0001 | c0001 | t0015 | g0184 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0245 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0255 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02683 | hp1 | a0001 | c0001 | t0007 | g0204 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02698 | hp2 | a0001 | c0001 | t0044 | g0222 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02717 | hp1 | a0001 | c0002 | t0008 | g0074 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02717 | hp2 | a0001 | c0003 | t0004 | g0052 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02723 | hp1 | a0001 | c0003 | t0023 | g0045 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02723 | hp2 | a0001 | c0003 | t0022 | g0200 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02735 | hp1 | a0001 | c0003 | t0003 | g0147 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02735 | hp2 | a0001 | c0001 | t0014 | g0226 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0111 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02738 | hp2 | a0001 | c0001 | t0010 | g0201 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0246 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02809 | hp2 | a0001 | c0002 | t0051 | g0041 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02818 | hp2 | a0001 | c0001 | t0011 | g0188 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02886 | hp1 | a0001 | c0003 | t0003 | g0027 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02886 | hp2 | a0001 | c0003 | t0020 | g0179 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0243 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02896 | hp1 | a0001 | c0001 | t0052 | g0040 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02896 | hp2 | a0001 | c0003 | t0003 | g0003 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02897 | hp1 | a0001 | c0003 | t0003 | g0003 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0242 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02922 | hp1 | a0001 | c0001 | t0015 | g0015 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0195 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0240 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02965 | hp2 | a0001 | c0002 | t0008 | g0198 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02970 | hp1 | a0001 | c0003 | t0037 | g0050 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02970 | hp2 | a0001 | c0001 | t0035 | g0024 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02976 | hp1 | a0001 | c0002 | t0009 | g0098 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02976 | hp2 | a0001 | c0001 | t0025 | g0004 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03041 | hp2 | a0001 | c0003 | t0022 | g0199 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03098 | hp1 | a0001 | c0003 | t0003 | g0026 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03098 | hp2 | a0001 | c0003 | t0004 | g0056 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03130 | hp2 | a0001 | c0003 | t0004 | g0053 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03139 | hp1 | a0001 | c0003 | t0003 | g0265 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03139 | hp2 | a0001 | c0003 | t0004 | g0057 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03195 | hp1 | a0001 | c0001 | t0038 | g0017 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03195 | hp2 | a0001 | c0003 | t0004 | g0049 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0239 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03225 | hp2 | a0001 | c0002 | t0009 | g0101 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0238 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03486 | hp1 | a0001 | c0004 | t0002 | g0073 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03486 | hp2 | a0001 | c0003 | t0004 | g0054 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03490 | hp1 | a0001 | c0001 | t0047 | g0202 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0063 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03491 | hp1 | a0001 | c0001 | t0013 | g0229 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0071 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03516 | hp2 | a0001 | c0003 | t0004 | g0046 | AFR | ESN | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03540 | hp1 | a0001 | c0001 | t0012 | g0252 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0236 | AFR | GWD | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03579 | hp2 | a0001 | c0001 | t0045 | g0268 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0104 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03688 | hp1 | a0001 | c0001 | t0016 | g0218 | SAS | STU | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03704 | hp1 | a0001 | c0001 | t0048 | g0217 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03704 | hp2 | a0001 | c0003 | t0003 | g0257 | SAS | PJL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03831 | hp1 | a0001 | c0001 | t0024 | g0210 | SAS | BEB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03834 | hp2 | a0001 | c0001 | t0010 | g0216 | SAS | BEB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03927 | hp1 | a0001 | c0001 | t0027 | g0215 | SAS | BEB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03927 | hp2 | a0001 | c0003 | t0003 | g0260 | SAS | BEB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG04115 | hp2 | a0001 | c0001 | t0024 | g0214 | SAS | STU | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG04204 | hp2 | a0001 | c0003 | t0003 | g0259 | SAS | STU | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG04228 | hp1 | a0001 | c0001 | t0031 | g0234 | SAS | STU | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0110 | SAS | STU | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0187 | AFR | YRI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18522 | hp2 | a0001 | c0001 | t0034 | g0233 | AFR | YRI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0078 | EAS | CHB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | CHB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18906 | hp1 | a0001 | c0001 | t0012 | g0250 | AFR | YRI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0189 | AFR | YRI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18940 | hp1 | a0001 | c0003 | t0039 | g0025 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18943 | hp2 | a0001 | c0002 | t0008 | g0088 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18965 | hp2 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18974 | hp1 | a0001 | c0006 | t0046 | g0212 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18982 | hp1 | a0001 | c0003 | t0003 | g0033 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18984 | hp2 | a0001 | c0003 | t0003 | g0023 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18989 | hp2 | a0001 | c0003 | t0003 | g0036 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18994 | hp2 | a0001 | c0003 | t0003 | g0035 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19003 | hp2 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19009 | hp2 | a0001 | c0003 | t0003 | g0031 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19030 | hp1 | a0001 | c0003 | t0020 | g0180 | AFR | LWK | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19030 | hp2 | a0001 | c0002 | t0008 | g0196 | AFR | LWK | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19043 | hp1 | a0001 | c0002 | t0008 | g0197 | AFR | LWK | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19043 | hp2 | a0002 | c0005 | t0012 | g0251 | AFR | LWK | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19058 | hp2 | a0001 | c0001 | t0013 | g0016 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19066 | hp2 | a0001 | c0003 | t0003 | g0034 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19068 | hp1 | a0001 | c0001 | t0021 | g0016 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19074 | hp2 | a0001 | c0001 | t0026 | g0132 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19084 | hp1 | a0001 | c0001 | t0021 | g0219 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19240 | hp1 | a0001 | c0002 | t0009 | g0100 | AFR | YRI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0192 | AFR | YRI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA20129 | hp1 | a0001 | c0003 | t0003 | g0028 | AFR | ASW | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0194 | AFR | ASW | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA20752 | hp1 | a0001 | c0001 | t0013 | g0249 | EUR | TSI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA20752 | hp2 | a0001 | c0003 | t0003 | g0038 | EUR | TSI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0067 | EUR | TSI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | TSI | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | GIH | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA20905 | hp2 | a0001 | c0003 | t0049 | g0258 | SAS | GIH | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02109 | hp2 | a0001 | c0002 | t0009 | g0099 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02486 | hp1 | a0001 | c0003 | t0004 | g0044 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0247 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02559 | hp1 | a0001 | c0003 | t0004 | g0006 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0227 | AFR | ACB | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03471 | hp1 | a0001 | c0003 | t0004 | g0006 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0185 | AFR | MSL | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG06807 | hp1 | a0001 | c0001 | t0042 | g0256 | AFR | USA | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | USA | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | USA | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA20300 | hp2 | a0001 | c0001 | t0033 | g0267 | AFR | USA | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA21309 | hp1 | a0001 | c0001 | t0025 | g0004 | AFR | LWK | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| NA21309 | hp2 | a0001 | c0003 | t0004 | g0043 | AFR | LWK | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0007 | g0105 | REF | REF | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0018 | REF | REF | CLCN3_chr4_169615578_169728673 | CLCN3 | chr4 | 169615578 | 169728673 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:169713141 | A | G | 1 | a0002 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.2212A>G | p.Thr738Ala | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/13 | 2714/6635 | 2212/2457 | 738/818 | chr4 | 169713141 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:169636045 | A | G | 1 | a0001c0008 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.117A>G | p.Gln39Gln | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/13 | 619/6635 | 117/2457 | 39/818 | chr4 | 169636045 | |||
| chr4:169689230 | G | A | 1 | a0001c0004 | 1 | HG03486.hp1 | splice_region_variant&synonymous_variant | LOW | c.606G>A | p.Glu202Glu | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/13 | 1108/6635 | 606/2457 | 202/818 | chr4 | 169689230 | |||
| chr4:169707085 | C | T | 1 | a0001c0007 | 1 | HG00733.hp1 | synonymous_variant | LOW | c.1968C>T | p.Asp656Asp | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/13 | 2470/6635 | 1968/2457 | 656/818 | chr4 | 169707085 | |||
| chr4:169707241 | C | T | 1 | a0001c0006 | 1 | NA18974.hp1 | synonymous_variant | LOW | c.2124C>T | p.Leu708Leu | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/13 | 2626/6635 | 2124/2457 | 708/818 | chr4 | 169707241 | |||
| chr4:169713239 | C | T | 2 | a0001c0002 a0001c0004 |
67 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(64): Show |
synonymous_variant | LOW | c.2310C>T | p.Ile770Ile | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/13 | 2812/6635 | 2310/2457 | 770/818 | chr4 | 169713239 | |||
| chr4:169713257 | A | G | 1 | a0001c0003 | 50 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(47): Show |
synonymous_variant | LOW | c.2328A>G | p.Arg776Arg | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/13 | 2830/6635 | 2328/2457 | 776/818 | chr4 | 169713257 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:169620578 | C | G | 1 | a0001c0001t0025 | 2 | HG02976.hp2 NA21309.hp1 |
5_prime_UTR_variant | MODIFIER | c.-502C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/13 | 15351 | chr4 | 169620578 | ||||||
| chr4:169620589 | C | T | 1 | a0001c0001t0024 | 2 | HG03831.hp1 HG04115.hp2 |
5_prime_UTR_variant | MODIFIER | c.-491C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/13 | 15340 | chr4 | 169620589 | ||||||
| chr4:169620632 | C | G | 2 | a0001c0001t0052 a0001c0002t0051 |
2 | HG02809.hp2 HG02896.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-448C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/13 | chr4 | 169620632 | |||||||
| chr4:169635918 | C | T | 1 | a0001c0002t0050 | 1 | HG01069.hp2 | 5_prime_UTR_variant | MODIFIER | c.-11C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/13 | 11 | chr4 | 169635918 | ||||||
| chr4:169720232 | G | A | 1 | a0001c0001t0026 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*235G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 235 | chr4 | 169720232 | ||||||
| chr4:169720243 | A | G | 1 | a0001c0003t0049 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*246A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 246 | chr4 | 169720243 | ||||||
| chr4:169720361 | A | G | 1 | a0001c0002t0017 | 3 | HG01257.hp1 HG01258.hp2 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*364A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 364 | chr4 | 169720361 | ||||||
| chr4:169720526 | T | TCTCTCTC others(6): Show |
1 | a0001c0001t0027 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*529_*530insCTCTCT others(7): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 530 | chr4 | 169720526 | ||||||
| chr4:169720526 | T | TCTCTCTC others(14): Show |
1 | a0001c0001t0028 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*529_*530insCTCTCT others(15): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 530 | chr4 | 169720526 | ||||||
| chr4:169720526 | T | TTC | 7 | a0001c0001t0038 a0001c0001t0042 a0001c0001t0043 others(4): Show |
7 | HG01261.hp2 HG02280.hp1 HG02602.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*561_*562dupCT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | |||||
| chr4:169720526 | T | TTCTCTC | 2 | a0001c0001t0012 a0002c0005t0012 |
4 | HG02486.hp2 HG03540.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*557_*562dupCTCTCT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | |||||
| chr4:169720526 | T | TTCTCTCT others(3): Show |
2 | a0001c0001t0013 a0001c0001t0044 |
5 | HG01433.hp2 HG02698.hp2 HG03491.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*553_*562dupCTCTCT others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | |||||
| chr4:169720526 | T | TTCTCTCT others(5): Show |
2 | a0001c0001t0014 a0001c0001t0045 |
5 | HG01099.hp1 HG01243.hp1 HG01517.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*551_*562dupCTCTCT others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | |||||
| chr4:169720526 | T | TTCTCTCT others(7): Show |
1 | a0001c0001t0010 | 5 | HG00738.hp1 HG01168.hp2 HG01255.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*549_*562dupCTCTCT others(8): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | |||||
| chr4:169720526 | T | TTCTCTCT others(9): Show |
2 | a0001c0001t0007 a0001c0001t0052 |
8 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*547_*562dupCTCTCT others(10): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | |||||
| chr4:169720526 | T | TTCTCTCT others(11): Show |
1 | a0001c0001t0016 | 3 | HG02040.hp2 HG02602.hp1 HG03688.hp1 |
3_prime_UTR_variant | MODIFIER | c.*545_*562dupCTCTCT others(12): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | |||||
| chr4:169720526 | T | TTCTCTCT others(13): Show |
2 | a0001c0001t0024 a0001c0006t0046 |
3 | HG03831.hp1 HG04115.hp2 NA18974.hp1 |
3_prime_UTR_variant | MODIFIER | c.*543_*562dupCTCTCT others(14): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | |||||
| chr4:169720526 | T | TTCTCTCT others(19): Show |
1 | a0001c0001t0047 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*537_*562dupCTCTCT others(20): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | |||||
| chr4:169720526 | T | TTCTCTCT others(21): Show |
1 | a0001c0001t0048 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*535_*562dupCTCTCT others(22): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 563 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | |||||
| chr4:169720526 | TTC | T | 7 | a0001c0001t0015 a0001c0001t0021 a0001c0002t0008 others(4): Show |
34 | HG00639.hp2 HG01175.hp2 HG01496.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*561_*562delCT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 561 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | |||||
| chr4:169720526 | TTCTC | T | 8 | a0001c0001t0001 a0001c0001t0018 a0001c0001t0019 others(5): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*559_*562delCTCT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 559 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | |||||
| chr4:169720526 | TTCTCTCT others(3): Show |
T | 1 | a0001c0001t0011 | 4 | HG02572.hp1 HG02818.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*553_*562delCTCTCT others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 553 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | |||||
| chr4:169720526 | TTCTCTCT others(9): Show |
T | 1 | a0001c0003t0029 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*547_*562delCTCTCT others(10): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 547 | INFO_REALIGN_3_PRIME | chr4 | 169720526 | |||||
| chr4:169720923 | C | G | 2 | a0001c0001t0006 a0001c0001t0043 |
9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*926C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 926 | chr4 | 169720923 | ||||||
| chr4:169721095 | A | G | 7 | a0001c0001t0001 a0001c0001t0018 a0001c0001t0019 others(4): Show |
93 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1098A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1098 | chr4 | 169721095 | ||||||
| chr4:169721150 | A | AT | 2 | a0001c0001t0006 a0001c0001t0043 |
9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1161dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1162 | INFO_REALIGN_3_PRIME | chr4 | 169721150 | |||||
| chr4:169721339 | T | G | 1 | a0001c0003t0022 | 2 | HG02723.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1342T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1342 | chr4 | 169721339 | ||||||
| chr4:169721411 | T | C | 1 | a0001c0001t0031 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1414T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1414 | chr4 | 169721411 | ||||||
| chr4:169721508 | C | T | 1 | a0001c0001t0042 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1511C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1511 | chr4 | 169721508 | ||||||
| chr4:169721509 | G | A | 2 | a0001c0001t0011 a0001c0001t0015 |
7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1512G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1512 | chr4 | 169721509 | ||||||
| chr4:169721530 | T | TA | 7 | a0001c0001t0025 a0001c0003t0004 a0001c0003t0020 others(4): Show |
25 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1543dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1544 | INFO_REALIGN_3_PRIME | chr4 | 169721530 | |||||
| chr4:169721618 | C | T | 2 | a0001c0001t0012 a0002c0005t0012 |
4 | HG02486.hp2 HG03540.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1621C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1621 | chr4 | 169721618 | ||||||
| chr4:169721630 | C | T | 12 | a0001c0001t0006 a0001c0001t0042 a0001c0001t0043 others(9): Show |
77 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1633C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1633 | chr4 | 169721630 | ||||||
| chr4:169721683 | G | T | 52 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(49): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*1686G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1686 | chr4 | 169721683 | ||||||
| chr4:169721899 | G | A | 2 | a0001c0001t0033 a0001c0001t0045 |
2 | HG03579.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1902G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1902 | chr4 | 169721899 | ||||||
| chr4:169721937 | C | T | 1 | a0001c0001t0035 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1940C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 1940 | chr4 | 169721937 | ||||||
| chr4:169722149 | A | G | 1 | a0001c0002t0036 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2152A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 2152 | chr4 | 169722149 | ||||||
| chr4:169722564 | G | T | 1 | a0001c0001t0044 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2567G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 2567 | chr4 | 169722564 | ||||||
| chr4:169722566 | T | A | 1 | a0001c0001t0052 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2569T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 2569 | chr4 | 169722566 | ||||||
| chr4:169723039 | G | A | 1 | a0001c0001t0018 | 2 | HG00323.hp1 HG01261.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3042G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 3042 | chr4 | 169723039 | ||||||
| chr4:169723289 | A | G | 1 | a0001c0003t0020 | 2 | HG02886.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3292A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 3292 | chr4 | 169723289 | ||||||
| chr4:169723482 | AT | A | 9 | a0001c0001t0011 a0001c0001t0015 a0001c0001t0019 others(6): Show |
42 | HG01258.hp1 HG01346.hp1 HG01496.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*3498delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 3498 | INFO_REALIGN_3_PRIME | chr4 | 169723482 | |||||
| chr4:169723495 | T | C | 1 | a0001c0001t0032 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3498T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 13/13 | 3498 | chr4 | 169723495 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:169621146 | T | G | 1 | a0001c0003t0003g0003 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-17+83T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169621146 | |||||||
| chr4:169621162 | T | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-17+99T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169621162 | |||||||
| chr4:169621489 | A | T | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-17+426A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169621489 | |||||||
| chr4:169621547 | A | G | 13 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(10): Show |
14 | HG02280.hp1 HG02622.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-17+484A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169621547 | |||||||
| chr4:169621658 | G | T | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-17+595G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169621658 | |||||||
| chr4:169621707 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-17+644T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169621707 | |||||||
| chr4:169621876 | T | C | 1 | a0001c0001t0025g0004 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-17+813T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169621876 | |||||||
| chr4:169621927 | C | T | 1 | a0001c0001t0006g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-17+864C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169621927 | |||||||
| chr4:169622048 | A | T | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | NA18981.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-17+985A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622048 | |||||||
| chr4:169622050 | A | G | 3 | a0001c0001t0012g0250 a0001c0001t0012g0252 a0002c0005t0012g0251 |
3 | HG03540.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-17+987A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622050 | |||||||
| chr4:169622076 | C | G | 1 | a0001c0001t0013g0249 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-17+1013C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622076 | |||||||
| chr4:169622179 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-17+1116G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622179 | |||||||
| chr4:169622335 | C | T | 1 | a0001c0001t0043g0248 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-17+1272C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622335 | |||||||
| chr4:169622481 | G | A | 254 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(251): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-17+1418G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622481 | |||||||
| chr4:169622674 | G | T | 1 | a0001c0001t0031g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-17+1611G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622674 | |||||||
| chr4:169622685 | G | A | 1 | a0001c0001t0043g0248 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-17+1622G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622685 | |||||||
| chr4:169622813 | C | T | 1 | a0001c0001t0034g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-17+1750C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622813 | |||||||
| chr4:169622932 | C | T | 37 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0007g0204 others(34): Show |
37 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.-17+1869C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169622932 | |||||||
| chr4:169623083 | CAG | C | 35 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0007g0204 others(32): Show |
35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.-17+2026_-17+2027d others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169623083 | ||||||
| chr4:169623105 | T | C | 5 | a0001c0003t0003g0003 a0001c0003t0003g0257 a0001c0003t0003g0259 others(2): Show |
6 | HG02896.hp2 HG02897.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17+2042T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169623105 | |||||||
| chr4:169623161 | C | T | 223 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(220): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.-17+2098C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169623161 | |||||||
| chr4:169623295 | G | A | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-17+2232G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169623295 | |||||||
| chr4:169623398 | A | G | 3 | a0001c0002t0008g0196 a0001c0002t0008g0197 a0001c0002t0008g0198 |
3 | HG02965.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-17+2335A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169623398 | |||||||
| chr4:169623730 | T | A | 1 | a0001c0003t0003g0023 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-17+2667T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169623730 | |||||||
| chr4:169623853 | T | G | 2 | a0001c0001t0052g0040 a0001c0002t0051g0041 |
2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-17+2790T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169623853 | |||||||
| chr4:169623888 | T | C | 33 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(30): Show |
33 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.-17+2825T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169623888 | |||||||
| chr4:169623929 | T | G | 1 | a0001c0002t0002g0042 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-17+2866T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169623929 | |||||||
| chr4:169623944 | C | T | 1 | a0001c0002t0002g0042 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-17+2881C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169623944 | |||||||
| chr4:169624223 | T | C | 3 | a0001c0001t0010g0201 a0001c0001t0016g0203 a0001c0001t0047g0202 |
3 | HG02602.hp1 HG02738.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-17+3160T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624223 | |||||||
| chr4:169624268 | G | A | 53 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(50): Show |
54 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.-17+3205G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624268 | |||||||
| chr4:169624280 | C | T | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.-17+3217C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624280 | |||||||
| chr4:169624424 | G | A | 2 | a0001c0001t0025g0004 a0001c0001t0034g0233 |
3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-17+3361G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624424 | |||||||
| chr4:169624428 | C | T | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-17+3365C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624428 | |||||||
| chr4:169624546 | G | A | 112 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(109): Show |
119 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.-17+3483G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624546 | |||||||
| chr4:169624621 | T | C | 1 | a0001c0002t0008g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-17+3558T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624621 | |||||||
| chr4:169624624 | A | G | 9 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(6): Show |
9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.-17+3561A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624624 | |||||||
| chr4:169624663 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-17+3600G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624663 | |||||||
| chr4:169624936 | T | C | 6 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(3): Show |
6 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.-17+3873T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624936 | |||||||
| chr4:169624947 | A | G | 2 | a0001c0001t0052g0040 a0001c0002t0051g0041 |
2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-17+3884A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169624947 | |||||||
| chr4:169625280 | C | T | 151 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(148): Show |
161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-17+4217C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169625280 | |||||||
| chr4:169625358 | A | G | 151 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(148): Show |
161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-17+4295A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169625358 | |||||||
| chr4:169625358 | A | T | 1 | a0001c0001t0001g0014 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-17+4295A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169625358 | |||||||
| chr4:169625470 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-17+4407T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169625470 | |||||||
| chr4:169625524 | AG | A | 4 | a0001c0001t0012g0250 a0001c0001t0012g0252 a0001c0001t0042g0256 others(1): Show |
4 | HG03540.hp1 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17+4463delG | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169625524 | ||||||
| chr4:169625661 | G | A | 1 | a0001c0001t0033g0267 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-17+4598G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169625661 | |||||||
| chr4:169626144 | G | A | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.-17+5081G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626144 | |||||||
| chr4:169626154 | A | C | 1 | a0001c0002t0017g0008 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-17+5091A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626154 | |||||||
| chr4:169626195 | G | A | 3 | a0001c0001t0005g0236 a0001c0001t0030g0237 a0001c0008t0005g0235 |
3 | HG02055.hp1 HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-17+5132G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626195 | |||||||
| chr4:169626312 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-17+5249A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626312 | |||||||
| chr4:169626407 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-17+5344G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626407 | |||||||
| chr4:169626422 | G | A | 2 | a0001c0001t0025g0004 a0001c0001t0034g0233 |
3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-17+5359G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626422 | |||||||
| chr4:169626435 | G | A | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-17+5372G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626435 | |||||||
| chr4:169626482 | C | A | 253 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-17+5419C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626482 | |||||||
| chr4:169626506 | C | A | 1 | a0001c0001t0006g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-17+5443C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626506 | |||||||
| chr4:169626514 | C | A | 3 | a0001c0001t0005g0236 a0001c0001t0030g0237 a0001c0008t0005g0235 |
3 | HG02055.hp1 HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-17+5451C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626514 | |||||||
| chr4:169626569 | C | G | 1 | a0001c0001t0006g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-17+5506C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626569 | |||||||
| chr4:169626656 | G | A | 2 | a0001c0001t0025g0004 a0001c0001t0034g0233 |
3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-17+5593G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626656 | |||||||
| chr4:169626674 | A | C | 2 | a0001c0001t0052g0040 a0001c0002t0051g0041 |
2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-17+5611A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169626674 | |||||||
| chr4:169627296 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-17+6233C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169627296 | |||||||
| chr4:169627374 | G | T | 255 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(252): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-17+6311G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169627374 | |||||||
| chr4:169627386 | T | G | 1 | a0001c0001t0025g0004 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-17+6323T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169627386 | |||||||
| chr4:169628177 | A | G | 7 | a0001c0003t0004g0006 a0001c0003t0004g0054 a0001c0003t0004g0056 others(4): Show |
8 | HG00639.hp2 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17+7114A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169628177 | |||||||
| chr4:169628292 | G | A | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.-17+7229G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169628292 | |||||||
| chr4:169628661 | C | T | 18 | a0001c0003t0004g0006 a0001c0003t0004g0043 a0001c0003t0004g0044 others(15): Show |
19 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.-16-7252C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169628661 | |||||||
| chr4:169628709 | A | G | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.-16-7204A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169628709 | |||||||
| chr4:169628784 | A | G | 112 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(109): Show |
119 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.-16-7129A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169628784 | |||||||
| chr4:169628968 | G | C | 1 | a0001c0003t0039g0025 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-16-6945G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169628968 | |||||||
| chr4:169629017 | G | A | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-16-6896G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629017 | |||||||
| chr4:169629043 | A | G | 10 | a0001c0003t0004g0044 a0001c0003t0004g0046 a0001c0003t0004g0047 others(7): Show |
10 | HG01175.hp2 HG01358.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-16-6870A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629043 | |||||||
| chr4:169629142 | G | A | 1 | a0001c0002t0002g0060 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-16-6771G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629142 | |||||||
| chr4:169629176 | TCTGTATC others(4): Show |
T | 97 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(94): Show |
102 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.-16-6729_-16-6719d others(13): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169629176 | ||||||
| chr4:169629223 | A | G | 3 | a0001c0001t0012g0250 a0001c0001t0012g0252 a0002c0005t0012g0251 |
3 | HG03540.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-16-6690A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629223 | |||||||
| chr4:169629278 | A | AT | 112 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(109): Show |
119 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.-16-6628dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169629278 | ||||||
| chr4:169629529 | C | G | 1 | a0001c0001t0032g0181 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-16-6384C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629529 | |||||||
| chr4:169629663 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-16-6250G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629663 | |||||||
| chr4:169629674 | T | C | 35 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(32): Show |
35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.-16-6239T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629674 | |||||||
| chr4:169629713 | G | T | 1 | a0001c0002t0002g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-16-6200G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629713 | |||||||
| chr4:169629825 | A | G | 1 | a0001c0003t0004g0043 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-16-6088A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629825 | |||||||
| chr4:169629874 | G | A | 3 | a0001c0003t0003g0026 a0001c0003t0003g0027 a0001c0003t0003g0028 |
3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-16-6039G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169629874 | |||||||
| chr4:169630100 | TTGTAA | T | 39 | a0001c0001t0011g0185 a0001c0001t0011g0186 a0001c0001t0011g0187 others(36): Show |
43 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(40): Show |
intron_variant | MODIFIER | c.-16-5812_-16-5808d others(7): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630100 | |||||||
| chr4:169630174 | T | G | 1 | a0001c0001t0007g0204 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-16-5739T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630174 | |||||||
| chr4:169630209 | T | G | 59 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(56): Show |
65 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.-16-5704T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630209 | |||||||
| chr4:169630222 | T | C | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.-16-5691T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630222 | |||||||
| chr4:169630227 | A | G | 3 | a0001c0001t0005g0244 a0001c0001t0005g0245 a0001c0001t0005g0246 |
3 | HG02622.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-16-5686A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630227 | |||||||
| chr4:169630289 | G | T | 254 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(251): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-16-5624G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630289 | |||||||
| chr4:169630294 | C | T | 1 | a0001c0003t0004g0059 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-16-5619C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630294 | |||||||
| chr4:169630332 | A | G | 260 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(257): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-16-5581A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630332 | |||||||
| chr4:169630346 | G | C | 15 | a0001c0001t0011g0185 a0001c0001t0011g0186 a0001c0001t0011g0187 others(12): Show |
17 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.-16-5567G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630346 | |||||||
| chr4:169630421 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-16-5492A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630421 | |||||||
| chr4:169630473 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-16-5440T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630473 | |||||||
| chr4:169630560 | T | G | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-16-5353T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630560 | |||||||
| chr4:169630676 | AC | A | 2 | a0001c0001t0025g0004 a0001c0001t0034g0233 |
3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-16-5235delC | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169630676 | ||||||
| chr4:169630772 | G | A | 1 | a0001c0001t0012g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-16-5141G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630772 | |||||||
| chr4:169630784 | C | T | 1 | a0001c0001t0012g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-16-5129C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630784 | |||||||
| chr4:169630819 | G | A | 13 | a0001c0003t0003g0005 a0001c0003t0003g0023 a0001c0003t0003g0029 others(10): Show |
14 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.-16-5094G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630819 | |||||||
| chr4:169630855 | A | G | 1 | a0001c0002t0002g0110 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-16-5058A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169630855 | |||||||
| chr4:169631008 | G | GT | 2 | a0001c0001t0025g0004 a0001c0001t0034g0233 |
3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-16-4901dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169631008 | ||||||
| chr4:169631186 | T | C | 1 | a0001c0003t0003g0029 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-16-4727T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631186 | |||||||
| chr4:169631286 | TTTTG | T | 6 | a0001c0001t0011g0185 a0001c0001t0011g0186 a0001c0001t0011g0187 others(3): Show |
7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-16-4616_-16-4613d others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169631286 | ||||||
| chr4:169631410 | C | T | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-16-4503C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631410 | |||||||
| chr4:169631481 | G | T | 92 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(89): Show |
97 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.-16-4432G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631481 | |||||||
| chr4:169631489 | C | T | 1 | a0001c0001t0034g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-16-4424C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631489 | |||||||
| chr4:169631735 | A | G | 253 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-16-4178A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631735 | |||||||
| chr4:169631834 | G | A | 253 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-16-4079G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631834 | |||||||
| chr4:169631850 | G | A | 253 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-16-4063G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631850 | |||||||
| chr4:169631858 | A | G | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-16-4055A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631858 | |||||||
| chr4:169631933 | C | T | 1 | a0001c0001t0005g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-16-3980C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631933 | |||||||
| chr4:169631960 | A | C | 1 | a0001c0003t0003g0003 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-16-3953A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169631960 | |||||||
| chr4:169632199 | GATCCA | G | 92 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(89): Show |
97 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.-16-3713_-16-3709d others(7): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169632199 | |||||||
| chr4:169632362 | C | T | 1 | a0001c0002t0002g0109 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-16-3551C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169632362 | |||||||
| chr4:169632408 | C | T | 33 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(30): Show |
33 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.-16-3505C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169632408 | |||||||
| chr4:169632409 | C | T | 3 | a0001c0001t0001g0177 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | NA18981.hp2 NA18986.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-16-3504C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169632409 | |||||||
| chr4:169632686 | C | A | 1 | a0001c0002t0009g0061 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-16-3227C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169632686 | |||||||
| chr4:169632716 | C | CA | 96 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(93): Show |
99 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.-16-3171dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169632716 | ||||||
| chr4:169632716 | C | CAA | 14 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0019 others(11): Show |
16 | HG00544.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-16-3172_-16-3171d others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169632716 | ||||||
| chr4:169632716 | CA | C | 20 | a0001c0001t0011g0185 a0001c0001t0011g0186 a0001c0001t0015g0184 others(17): Show |
21 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-16-3171delA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169632716 | ||||||
| chr4:169632716 | CAA | C | 6 | a0001c0001t0011g0187 a0001c0001t0011g0188 a0001c0001t0015g0015 others(3): Show |
7 | HG02451.hp1 HG02615.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16-3172_-16-3171d others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169632716 | ||||||
| chr4:169632716 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0052g0040 a0001c0002t0051g0041 |
2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-16-3181_-16-3171d others(13): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169632716 | ||||||
| chr4:169632716 | CAAAAAAA others(7): Show |
C | 1 | a0001c0002t0008g0108 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-16-3184_-16-3171d others(16): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169632716 | ||||||
| chr4:169632841 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-16-3072A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169632841 | |||||||
| chr4:169632843 | C | A | 2 | a0001c0001t0052g0040 a0001c0002t0051g0041 |
2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-16-3070C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169632843 | |||||||
| chr4:169632947 | T | A | 3 | a0001c0001t0033g0267 a0001c0001t0045g0268 a0001c0003t0003g0265 |
3 | HG03139.hp1 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-16-2966T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169632947 | |||||||
| chr4:169633035 | CAG | C | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.-16-2875_-16-2874d others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169633035 | ||||||
| chr4:169633068 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG00544.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.-16-2845A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169633068 | |||||||
| chr4:169633262 | C | T | 1 | a0001c0002t0050g0106 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-16-2651C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169633262 | |||||||
| chr4:169633411 | A | G | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-16-2502A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169633411 | |||||||
| chr4:169633488 | TG | T | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.-16-2424delG | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169633488 | |||||||
| chr4:169633613 | A | G | 1 | a0001c0001t0031g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-16-2300A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169633613 | |||||||
| chr4:169633763 | G | A | 2 | a0001c0001t0052g0040 a0001c0002t0051g0041 |
2 | HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-16-2150G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169633763 | |||||||
| chr4:169633888 | G | A | 1 | a0001c0004t0002g0073 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-16-2025G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169633888 | |||||||
| chr4:169633906 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-16-2007G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169633906 | |||||||
| chr4:169633954 | GT | G | 251 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(248): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-16-1947delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 169633954 | ||||||
| chr4:169633970 | T | C | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.-16-1943T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169633970 | |||||||
| chr4:169634032 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-16-1881G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169634032 | |||||||
| chr4:169634113 | C | T | 2 | a0001c0001t0025g0004 a0001c0001t0034g0233 |
3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-16-1800C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169634113 | |||||||
| chr4:169634258 | T | C | 59 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(56): Show |
65 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.-16-1655T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169634258 | |||||||
| chr4:169634349 | A | T | 1 | a0001c0001t0001g0173 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-16-1564A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169634349 | |||||||
| chr4:169634415 | T | C | 1 | a0001c0001t0016g0211 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-16-1498T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169634415 | |||||||
| chr4:169634591 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-16-1322A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169634591 | |||||||
| chr4:169634773 | T | C | 2 | a0001c0001t0025g0004 a0001c0001t0034g0233 |
3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-16-1140T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169634773 | |||||||
| chr4:169634893 | T | C | 1 | a0001c0003t0004g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-16-1020T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169634893 | |||||||
| chr4:169634970 | G | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0167 a0001c0001t0018g0166 others(1): Show |
5 | HG00323.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16-943G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169634970 | |||||||
| chr4:169635037 | G | A | 6 | a0001c0001t0005g0017 a0001c0001t0005g0238 a0001c0001t0005g0239 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16-876G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169635037 | |||||||
| chr4:169635479 | T | A | 1 | a0001c0001t0043g0248 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-16-434T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169635479 | |||||||
| chr4:169635519 | C | G | 1 | a0001c0001t0001g0165 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-16-394C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169635519 | |||||||
| chr4:169635695 | G | T | 147 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(144): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.-16-218G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169635695 | |||||||
| chr4:169635787 | A | G | 1 | a0001c0001t0045g0268 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-16-126A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169635787 | |||||||
| chr4:169635803 | C | T | 1 | a0001c0001t0035g0024 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-16-110C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169635803 | |||||||
| chr4:169635873 | A | C | 1 | a0001c0002t0002g0103 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-16-40A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 1/12 | chr4 | 169635873 | |||||||
| chr4:169636158 | T | A | 1 | a0001c0001t0047g0202 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.160+70T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636158 | |||||||
| chr4:169636231 | G | C | 3 | a0001c0001t0012g0250 a0001c0001t0012g0252 a0002c0005t0012g0251 |
3 | HG03540.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160+143G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636231 | |||||||
| chr4:169636315 | A | G | 11 | a0001c0003t0004g0043 a0001c0003t0004g0044 a0001c0003t0004g0046 others(8): Show |
11 | HG01175.hp2 HG01358.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.160+227A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636315 | |||||||
| chr4:169636399 | T | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0167 a0001c0001t0018g0166 others(1): Show |
5 | HG00323.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+311T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636399 | |||||||
| chr4:169636424 | T | G | 2 | a0001c0001t0012g0250 a0002c0005t0012g0251 |
2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160+336T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636424 | |||||||
| chr4:169636533 | A | C | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+445A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636533 | |||||||
| chr4:169636558 | G | T | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+470G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636558 | |||||||
| chr4:169636630 | T | C | 1 | a0001c0003t0003g0029 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.160+542T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636630 | |||||||
| chr4:169636734 | G | GGTT | 78 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0127 others(75): Show |
86 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.160+647_160+649dup others(3): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169636734 | ||||||
| chr4:169636735 | G | GT | 33 | a0001c0001t0005g0017 a0001c0001t0005g0236 a0001c0001t0005g0238 others(30): Show |
34 | HG00639.hp2 HG01109.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.160+663dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169636735 | ||||||
| chr4:169636735 | G | GTTGT | 91 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(88): Show |
98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.160+649_160+650ins others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169636735 | ||||||
| chr4:169636735 | G | GTTGTT | 16 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0006g0189 others(13): Show |
16 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.160+649_160+650ins others(5): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169636735 | ||||||
| chr4:169636737 | T | TG | 3 | a0001c0003t0003g0027 a0001c0003t0003g0028 a0001c0003t0003g0039 |
3 | HG02055.hp2 HG02886.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.160+649_160+650ins others(1): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636737 | |||||||
| chr4:169636881 | C | T | 53 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(50): Show |
54 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.160+793C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636881 | |||||||
| chr4:169636901 | T | C | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+813T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636901 | |||||||
| chr4:169636940 | C | G | 4 | a0001c0002t0008g0196 a0001c0002t0008g0197 a0001c0002t0008g0198 others(1): Show |
4 | HG02809.hp2 HG02965.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+852C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169636940 | |||||||
| chr4:169637287 | A | AT | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.160+1207dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169637287 | ||||||
| chr4:169637418 | C | T | 260 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(257): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.160+1330C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169637418 | |||||||
| chr4:169637453 | G | A | 200 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(197): Show |
215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.160+1365G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169637453 | |||||||
| chr4:169637565 | G | A | 25 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(22): Show |
27 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.160+1477G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169637565 | |||||||
| chr4:169637583 | A | ACAC | 175 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(172): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.160+1507_160+1509d others(5): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169637583 | ||||||
| chr4:169637595 | C | A | 1 | a0001c0003t0040g0266 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.160+1507C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169637595 | |||||||
| chr4:169637595 | C | CCAA | 77 | a0001c0001t0001g0010 a0001c0001t0007g0204 a0001c0001t0007g0205 others(74): Show |
81 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.160+1520_160+1522d others(5): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169637595 | ||||||
| chr4:169637598 | A | C | 3 | a0001c0001t0001g0159 a0001c0003t0020g0179 a0001c0003t0020g0180 |
3 | HG02886.hp2 NA18965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.160+1510A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169637598 | |||||||
| chr4:169637633 | C | G | 1 | a0001c0003t0022g0200 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.160+1545C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169637633 | |||||||
| chr4:169637745 | G | A | 200 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(197): Show |
215 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.160+1657G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169637745 | |||||||
| chr4:169637774 | A | G | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+1686A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169637774 | |||||||
| chr4:169638135 | G | T | 1 | a0001c0001t0025g0004 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.160+2047G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638135 | |||||||
| chr4:169638265 | G | T | 1 | a0001c0003t0003g0265 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.160+2177G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638265 | |||||||
| chr4:169638289 | T | C | 41 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0022 others(38): Show |
43 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.160+2201T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638289 | |||||||
| chr4:169638357 | A | G | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+2269A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638357 | |||||||
| chr4:169638405 | T | C | 3 | a0001c0001t0012g0250 a0001c0001t0012g0252 a0002c0005t0012g0251 |
3 | HG03540.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160+2317T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638405 | |||||||
| chr4:169638488 | A | AT | 199 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(196): Show |
214 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.160+2408dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169638488 | ||||||
| chr4:169638506 | A | G | 1 | a0001c0001t0052g0040 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.160+2418A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638506 | |||||||
| chr4:169638639 | G | A | 1 | a0001c0003t0004g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+2551G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638639 | |||||||
| chr4:169638680 | C | T | 1 | a0001c0001t0007g0209 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.160+2592C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638680 | |||||||
| chr4:169638791 | T | C | 3 | a0001c0001t0012g0250 a0001c0001t0012g0252 a0002c0005t0012g0251 |
3 | HG03540.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160+2703T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638791 | |||||||
| chr4:169638817 | C | G | 1 | a0001c0002t0002g0096 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.160+2729C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638817 | |||||||
| chr4:169638979 | C | T | 2 | a0001c0001t0025g0004 a0001c0001t0034g0233 |
3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.160+2891C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638979 | |||||||
| chr4:169638981 | A | G | 1 | a0001c0002t0002g0110 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.160+2893A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638981 | |||||||
| chr4:169638988 | A | C | 253 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.160+2900A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169638988 | |||||||
| chr4:169639180 | C | T | 92 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(89): Show |
97 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.160+3092C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169639180 | |||||||
| chr4:169639208 | T | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | NA18955.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.160+3120T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169639208 | |||||||
| chr4:169639511 | A | T | 1 | a0001c0001t0052g0040 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.160+3423A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169639511 | |||||||
| chr4:169639707 | A | G | 60 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(57): Show |
66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.160+3619A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169639707 | |||||||
| chr4:169639771 | A | G | 1 | a0001c0002t0002g0070 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.160+3683A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169639771 | |||||||
| chr4:169639965 | A | G | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0127 others(1): Show |
4 | HG01496.hp2 NA18956.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+3877A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169639965 | |||||||
| chr4:169639992 | T | C | 1 | a0001c0003t0003g0027 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.160+3904T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169639992 | |||||||
| chr4:169640008 | G | A | 20 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(17): Show |
22 | HG01884.hp1 HG02572.hp1 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.160+3920G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169640008 | |||||||
| chr4:169640531 | C | T | 17 | a0001c0003t0003g0005 a0001c0003t0003g0023 a0001c0003t0003g0026 others(14): Show |
18 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.160+4443C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169640531 | |||||||
| chr4:169640713 | T | C | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+4625T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169640713 | |||||||
| chr4:169640942 | C | G | 2 | a0001c0001t0001g0127 a0001c0001t0019g0126 |
2 | HG01496.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.160+4854C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169640942 | |||||||
| chr4:169640974 | C | G | 1 | a0001c0003t0003g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+4886C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169640974 | |||||||
| chr4:169641027 | T | C | 1 | a0001c0001t0052g0040 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.160+4939T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641027 | |||||||
| chr4:169641179 | C | T | 4 | a0001c0002t0008g0196 a0001c0002t0008g0197 a0001c0002t0008g0198 others(1): Show |
4 | HG02809.hp2 HG02965.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+5091C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641179 | |||||||
| chr4:169641447 | G | A | 53 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(50): Show |
54 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.160+5359G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641447 | |||||||
| chr4:169641490 | A | G | 1 | a0001c0001t0035g0024 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.160+5402A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641490 | |||||||
| chr4:169641550 | A | G | 7 | a0001c0002t0002g0069 a0001c0002t0002g0092 a0001c0002t0002g0093 others(4): Show |
7 | HG00558.hp1 HG00621.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.160+5462A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641550 | |||||||
| chr4:169641580 | A | C | 1 | a0001c0001t0006g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.160+5492A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641580 | |||||||
| chr4:169641607 | C | G | 1 | a0001c0003t0003g0260 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.160+5519C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641607 | |||||||
| chr4:169641633 | A | T | 153 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(150): Show |
164 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.160+5545A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641633 | |||||||
| chr4:169641975 | A | G | 92 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(89): Show |
97 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.160+5887A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641975 | |||||||
| chr4:169641984 | A | T | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.160+5896A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169641984 | |||||||
| chr4:169642002 | T | C | 208 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(205): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.160+5914T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169642002 | |||||||
| chr4:169642127 | T | A | 1 | a0001c0001t0001g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.160+6039T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169642127 | |||||||
| chr4:169642351 | C | T | 1 | a0001c0003t0037g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.160+6263C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169642351 | |||||||
| chr4:169642397 | C | T | 1 | a0001c0001t0052g0040 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.160+6309C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169642397 | |||||||
| chr4:169642582 | G | A | 53 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(50): Show |
54 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.160+6494G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169642582 | |||||||
| chr4:169642795 | C | T | 174 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(171): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.160+6707C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169642795 | |||||||
| chr4:169642833 | T | A | 1 | a0001c0001t0012g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.160+6745T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169642833 | |||||||
| chr4:169642934 | T | C | 260 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(257): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.160+6846T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169642934 | |||||||
| chr4:169643065 | G | A | 1 | a0001c0001t0012g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.160+6977G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169643065 | |||||||
| chr4:169643165 | A | G | 4 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0032g0181 others(1): Show |
4 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+7077A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169643165 | |||||||
| chr4:169643405 | T | C | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+7317T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169643405 | |||||||
| chr4:169643522 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.160+7434G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169643522 | |||||||
| chr4:169643546 | A | T | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+7458A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169643546 | |||||||
| chr4:169643618 | G | T | 1 | a0001c0001t0012g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.160+7530G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169643618 | |||||||
| chr4:169643698 | T | A | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+7610T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169643698 | |||||||
| chr4:169643960 | A | G | 4 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(1): Show |
4 | HG02622.hp1 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+7872A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169643960 | |||||||
| chr4:169644003 | G | T | 174 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(171): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.160+7915G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644003 | |||||||
| chr4:169644017 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.160+7929G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644017 | |||||||
| chr4:169644264 | T | C | 7 | a0001c0001t0011g0185 a0001c0001t0011g0186 a0001c0001t0011g0187 others(4): Show |
8 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+8176T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644264 | |||||||
| chr4:169644269 | C | CT | 9 | a0001c0002t0002g0068 a0001c0002t0002g0091 a0001c0003t0003g0003 others(6): Show |
10 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+8195dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169644269 | ||||||
| chr4:169644314 | G | A | 1 | a0001c0002t0002g0104 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.160+8226G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644314 | |||||||
| chr4:169644344 | G | A | 1 | a0001c0001t0024g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.160+8256G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644344 | |||||||
| chr4:169644368 | G | A | 1 | a0001c0002t0008g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.160+8280G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644368 | |||||||
| chr4:169644420 | G | A | 1 | a0001c0001t0013g0249 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.160+8332G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644420 | |||||||
| chr4:169644541 | C | T | 7 | a0001c0003t0003g0003 a0001c0003t0003g0257 a0001c0003t0003g0259 others(4): Show |
8 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+8453C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644541 | |||||||
| chr4:169644627 | C | T | 1 | a0001c0001t0034g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.160+8539C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644627 | |||||||
| chr4:169644699 | AC | A | 9 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(6): Show |
9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.160+8614delC | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169644699 | ||||||
| chr4:169644869 | T | C | 1 | a0001c0001t0028g0213 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.160+8781T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644869 | |||||||
| chr4:169644870 | G | A | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+8782G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169644870 | |||||||
| chr4:169645002 | C | A | 2 | a0001c0001t0025g0004 a0001c0001t0034g0233 |
3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.160+8914C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169645002 | |||||||
| chr4:169645055 | TG | T | 2 | a0001c0001t0025g0004 a0001c0001t0034g0233 |
3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.160+8968delG | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169645055 | |||||||
| chr4:169645067 | C | T | 1 | a0001c0001t0025g0004 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.160+8979C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169645067 | |||||||
| chr4:169645074 | T | C | 1 | a0001c0001t0052g0040 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.160+8986T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169645074 | |||||||
| chr4:169645157 | C | A | 35 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(32): Show |
35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.160+9069C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169645157 | |||||||
| chr4:169645284 | T | TTA | 7 | a0001c0003t0003g0003 a0001c0003t0003g0257 a0001c0003t0003g0259 others(4): Show |
8 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+9197_160+9198d others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169645284 | ||||||
| chr4:169645319 | C | G | 35 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(32): Show |
35 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.160+9231C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169645319 | |||||||
| chr4:169645823 | G | A | 1 | a0001c0002t0002g0075 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.160+9735G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169645823 | |||||||
| chr4:169646132 | A | G | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+10044A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169646132 | |||||||
| chr4:169646269 | G | A | 2 | a0001c0003t0020g0179 a0001c0003t0020g0180 |
2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.160+10181G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169646269 | |||||||
| chr4:169646395 | T | A | 60 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(57): Show |
66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.160+10307T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169646395 | |||||||
| chr4:169646683 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.160+10595T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169646683 | |||||||
| chr4:169646862 | A | C | 1 | a0001c0002t0002g0075 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.160+10774A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169646862 | |||||||
| chr4:169647215 | C | T | 33 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(30): Show |
33 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.160+11127C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169647215 | |||||||
| chr4:169647543 | A | G | 1 | a0001c0001t0052g0040 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.160+11455A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169647543 | |||||||
| chr4:169647638 | A | G | 176 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(173): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.160+11550A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169647638 | |||||||
| chr4:169647671 | T | C | 53 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(50): Show |
54 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.160+11583T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169647671 | |||||||
| chr4:169647753 | T | C | 1 | a0001c0001t0052g0040 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.160+11665T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169647753 | |||||||
| chr4:169648021 | C | T | 176 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(173): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.160+11933C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648021 | |||||||
| chr4:169648122 | A | G | 2 | a0001c0001t0025g0004 a0001c0001t0034g0233 |
3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.160+12034A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648122 | |||||||
| chr4:169648287 | G | A | 60 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(57): Show |
66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.160+12199G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648287 | |||||||
| chr4:169648330 | A | T | 176 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(173): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.160+12242A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648330 | |||||||
| chr4:169648393 | G | A | 1 | a0001c0001t0005g0242 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.160+12305G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648393 | |||||||
| chr4:169648428 | T | C | 53 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(50): Show |
54 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.160+12340T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648428 | |||||||
| chr4:169648567 | A | C | 1 | a0001c0001t0034g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.160+12479A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648567 | |||||||
| chr4:169648776 | C | T | 1 | a0001c0001t0006g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.160+12688C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648776 | |||||||
| chr4:169648811 | A | G | 229 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(226): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.160+12723A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648811 | |||||||
| chr4:169648894 | G | A | 1 | a0001c0001t0052g0040 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.160+12806G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648894 | |||||||
| chr4:169648942 | G | A | 11 | a0001c0001t0011g0185 a0001c0001t0011g0186 a0001c0001t0011g0187 others(8): Show |
13 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.160+12854G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648942 | |||||||
| chr4:169648972 | A | G | 1 | a0001c0002t0002g0096 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.160+12884A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169648972 | |||||||
| chr4:169649023 | T | TA | 12 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(9): Show |
12 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.160+12951dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169649023 | ||||||
| chr4:169649023 | TA | T | 117 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(114): Show |
124 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.160+12951delA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169649023 | ||||||
| chr4:169649087 | A | C | 1 | a0001c0001t0028g0213 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.160+12999A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169649087 | |||||||
| chr4:169649502 | A | G | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+13414A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169649502 | |||||||
| chr4:169649577 | A | T | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+13489A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169649577 | |||||||
| chr4:169649636 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.160+13548T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169649636 | |||||||
| chr4:169649702 | G | T | 7 | a0001c0003t0004g0006 a0001c0003t0004g0054 a0001c0003t0004g0056 others(4): Show |
8 | HG00639.hp2 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.160+13614G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169649702 | |||||||
| chr4:169649895 | G | A | 2 | a0001c0001t0007g0206 a0001c0001t0007g0209 |
2 | HG00323.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.160+13807G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169649895 | |||||||
| chr4:169649944 | G | A | 3 | a0001c0001t0001g0167 a0001c0001t0018g0166 a0001c0001t0018g0168 |
3 | HG00323.hp1 HG01074.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.160+13856G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169649944 | |||||||
| chr4:169649957 | C | T | 1 | a0001c0003t0022g0200 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.160+13869C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169649957 | |||||||
| chr4:169650060 | G | A | 3 | a0001c0001t0012g0250 a0001c0001t0012g0252 a0002c0005t0012g0251 |
3 | HG03540.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160+13972G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169650060 | |||||||
| chr4:169650373 | T | G | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+14285T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169650373 | |||||||
| chr4:169650609 | T | A | 260 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(257): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.160+14521T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169650609 | |||||||
| chr4:169650791 | A | C | 1 | a0001c0001t0001g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.160+14703A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169650791 | |||||||
| chr4:169650844 | A | G | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+14756A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169650844 | |||||||
| chr4:169651178 | T | G | 3 | a0001c0001t0001g0115 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | NA19068.hp2 NA19078.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.160+15090T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169651178 | |||||||
| chr4:169651221 | T | G | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+15133T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169651221 | |||||||
| chr4:169651554 | A | G | 1 | a0001c0002t0008g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.160+15466A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169651554 | |||||||
| chr4:169651667 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.160+15579G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169651667 | |||||||
| chr4:169651833 | T | A | 1 | a0001c0001t0026g0132 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.160+15745T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169651833 | |||||||
| chr4:169652136 | G | A | 2 | a0001c0003t0020g0179 a0001c0003t0020g0180 |
2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.160+16048G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169652136 | |||||||
| chr4:169652145 | A | G | 23 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(20): Show |
25 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(22): Show |
intron_variant | MODIFIER | c.160+16057A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169652145 | |||||||
| chr4:169652291 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.160+16203A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169652291 | |||||||
| chr4:169652446 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.160+16358G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169652446 | |||||||
| chr4:169652499 | T | A | 3 | a0001c0001t0001g0167 a0001c0001t0018g0166 a0001c0001t0018g0168 |
3 | HG00323.hp1 HG01074.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.160+16411T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169652499 | |||||||
| chr4:169652572 | G | A | 1 | a0001c0002t0002g0103 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.160+16484G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169652572 | |||||||
| chr4:169652795 | T | C | 1 | a0001c0002t0017g0008 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.160+16707T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169652795 | |||||||
| chr4:169653141 | C | T | 11 | a0001c0003t0004g0043 a0001c0003t0004g0044 a0001c0003t0004g0046 others(8): Show |
11 | HG01175.hp2 HG01358.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.160+17053C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653141 | |||||||
| chr4:169653148 | A | G | 6 | a0001c0001t0011g0185 a0001c0001t0011g0186 a0001c0001t0011g0187 others(3): Show |
7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+17060A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653148 | |||||||
| chr4:169653262 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.160+17174G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653262 | |||||||
| chr4:169653332 | C | T | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+17244C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653332 | |||||||
| chr4:169653514 | G | A | 7 | a0001c0003t0004g0006 a0001c0003t0004g0054 a0001c0003t0004g0056 others(4): Show |
8 | HG00639.hp2 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.160+17426G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653514 | |||||||
| chr4:169653553 | A | G | 1 | a0001c0001t0025g0004 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.160+17465A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653553 | |||||||
| chr4:169653640 | C | CA | 165 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(162): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.160+17573dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169653640 | ||||||
| chr4:169653640 | C | CAA | 45 | a0001c0001t0001g0125 a0001c0001t0001g0133 a0001c0001t0001g0134 others(42): Show |
45 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.160+17572_160+1757 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169653640 | ||||||
| chr4:169653640 | C | CAAA | 17 | a0001c0001t0011g0185 a0001c0001t0011g0186 a0001c0001t0011g0187 others(14): Show |
19 | HG00639.hp2 HG01884.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.160+17571_160+1757 others(7): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169653640 | ||||||
| chr4:169653677 | C | T | 2 | a0001c0003t0020g0179 a0001c0003t0020g0180 |
2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.160+17589C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653677 | |||||||
| chr4:169653678 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.160+17590G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653678 | |||||||
| chr4:169653777 | G | A | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+17689G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653777 | |||||||
| chr4:169653872 | A | G | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+17784A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169653872 | |||||||
| chr4:169654054 | A | C | 5 | a0001c0001t0005g0236 a0001c0001t0005g0242 a0001c0001t0005g0243 others(2): Show |
5 | HG02055.hp1 HG02258.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+17966A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654054 | |||||||
| chr4:169654092 | G | C | 58 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(55): Show |
64 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.160+18004G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654092 | |||||||
| chr4:169654162 | G | T | 1 | a0001c0001t0001g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.160+18074G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654162 | |||||||
| chr4:169654166 | G | A | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.160+18078G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654166 | |||||||
| chr4:169654234 | C | G | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+18146C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654234 | |||||||
| chr4:169654700 | C | T | 260 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(257): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.160+18612C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654700 | |||||||
| chr4:169654758 | A | T | 1 | a0001c0003t0003g0265 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.160+18670A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654758 | |||||||
| chr4:169654860 | A | G | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+18772A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654860 | |||||||
| chr4:169654918 | T | G | 46 | a0001c0001t0033g0267 a0001c0001t0045g0268 a0001c0003t0003g0003 others(43): Show |
49 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.160+18830T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654918 | |||||||
| chr4:169654948 | A | G | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.160+18860A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169654948 | |||||||
| chr4:169655059 | A | T | 1 | a0001c0001t0001g0178 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.160+18971A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169655059 | |||||||
| chr4:169655114 | A | G | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.160+19026A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169655114 | |||||||
| chr4:169655116 | A | G | 3 | a0001c0003t0003g0265 a0001c0003t0022g0199 a0001c0003t0022g0200 |
3 | HG02723.hp2 HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160+19028A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169655116 | |||||||
| chr4:169655192 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.160+19104T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169655192 | |||||||
| chr4:169655279 | C | T | 1 | a0001c0002t0050g0106 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.160+19191C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169655279 | |||||||
| chr4:169655623 | T | C | 26 | a0001c0001t0033g0267 a0001c0001t0045g0268 a0001c0003t0003g0003 others(23): Show |
28 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.160+19535T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169655623 | |||||||
| chr4:169655873 | C | T | 1 | a0001c0001t0012g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.160+19785C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169655873 | |||||||
| chr4:169656097 | C | T | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.160+20009C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656097 | |||||||
| chr4:169656103 | A | G | 5 | a0001c0002t0009g0061 a0001c0002t0009g0098 a0001c0002t0009g0099 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+20015A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656103 | |||||||
| chr4:169656268 | G | A | 1 | a0001c0008t0005g0235 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.160+20180G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656268 | |||||||
| chr4:169656269 | C | T | 2 | a0001c0003t0003g0005 a0001c0003t0003g0038 |
3 | HG01516.hp2 HG01517.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.160+20181C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656269 | |||||||
| chr4:169656279 | C | A | 1 | a0001c0001t0006g0189 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.160+20191C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656279 | |||||||
| chr4:169656439 | A | T | 2 | a0001c0001t0025g0004 a0001c0001t0034g0233 |
3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.160+20351A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656439 | |||||||
| chr4:169656488 | A | G | 9 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(6): Show |
9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.160+20400A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656488 | |||||||
| chr4:169656501 | C | A | 1 | a0001c0001t0001g0116 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.160+20413C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656501 | |||||||
| chr4:169656551 | G | A | 1 | a0001c0003t0023g0045 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.160+20463G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656551 | |||||||
| chr4:169656751 | C | T | 31 | a0001c0001t0005g0236 a0001c0001t0005g0242 a0001c0001t0005g0243 others(28): Show |
33 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(30): Show |
intron_variant | MODIFIER | c.160+20663C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656751 | |||||||
| chr4:169656828 | G | A | 1 | a0001c0001t0012g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.160+20740G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656828 | |||||||
| chr4:169656953 | T | C | 1 | a0001c0001t0034g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.160+20865T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169656953 | |||||||
| chr4:169657058 | A | G | 2 | a0001c0001t0010g0228 a0001c0001t0010g0230 |
2 | HG00738.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.160+20970A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169657058 | |||||||
| chr4:169657212 | A | G | 1 | a0001c0002t0008g0088 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.160+21124A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169657212 | |||||||
| chr4:169657270 | A | G | 50 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(47): Show |
56 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.160+21182A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169657270 | |||||||
| chr4:169657389 | T | C | 46 | a0001c0001t0033g0267 a0001c0001t0045g0268 a0001c0003t0003g0003 others(43): Show |
49 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.160+21301T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169657389 | |||||||
| chr4:169657471 | C | CA | 60 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(57): Show |
66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.160+21389dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169657471 | ||||||
| chr4:169657642 | G | C | 1 | a0001c0002t0002g0076 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.160+21554G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169657642 | |||||||
| chr4:169657644 | T | C | 1 | a0001c0002t0008g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.160+21556T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169657644 | |||||||
| chr4:169657774 | T | G | 1 | a0001c0001t0034g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.160+21686T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169657774 | |||||||
| chr4:169657851 | C | A | 97 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(94): Show |
103 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.160+21763C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169657851 | |||||||
| chr4:169658017 | G | C | 1 | a0001c0003t0003g0005 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.160+21929G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169658017 | |||||||
| chr4:169658183 | A | G | 1 | a0001c0003t0004g0049 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.161-21867A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169658183 | |||||||
| chr4:169658187 | G | T | 1 | a0001c0001t0005g0240 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.161-21863G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169658187 | |||||||
| chr4:169658224 | ATATAAT | A | 2 | a0001c0001t0025g0004 a0001c0001t0034g0233 |
3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.161-21821_161-2181 others(10): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169658224 | ||||||
| chr4:169658232 | A | T | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-21818A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169658232 | |||||||
| chr4:169658239 | TATATA | T | 61 | a0001c0001t0042g0256 a0001c0002t0002g0001 a0001c0002t0002g0002 others(58): Show |
67 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.161-21810_161-2180 others(9): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169658239 | |||||||
| chr4:169658248 | T | C | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.161-21802T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169658248 | |||||||
| chr4:169658308 | A | G | 3 | a0001c0001t0033g0267 a0001c0001t0034g0233 a0001c0001t0045g0268 |
3 | HG03579.hp2 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-21742A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169658308 | |||||||
| chr4:169658434 | A | G | 61 | a0001c0001t0042g0256 a0001c0002t0002g0001 a0001c0002t0002g0002 others(58): Show |
67 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.161-21616A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169658434 | |||||||
| chr4:169659053 | G | A | 2 | a0001c0002t0002g0077 a0001c0002t0002g0091 |
2 | NA18956.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.161-20997G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659053 | |||||||
| chr4:169659094 | A | C | 2 | a0001c0001t0006g0193 a0001c0001t0006g0194 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.161-20956A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659094 | |||||||
| chr4:169659160 | TG | T | 5 | a0001c0001t0005g0236 a0001c0001t0005g0242 a0001c0001t0005g0243 others(2): Show |
5 | HG02055.hp1 HG02258.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-20889delG | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659160 | |||||||
| chr4:169659176 | T | C | 2 | a0001c0001t0025g0004 a0001c0001t0034g0233 |
3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.161-20874T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659176 | |||||||
| chr4:169659276 | G | A | 1 | a0001c0003t0003g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.161-20774G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659276 | |||||||
| chr4:169659377 | A | T | 2 | a0001c0003t0020g0179 a0001c0003t0020g0180 |
2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.161-20673A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659377 | |||||||
| chr4:169659486 | C | T | 141 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(138): Show |
150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.161-20564C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659486 | |||||||
| chr4:169659626 | C | T | 26 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(23): Show |
28 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.161-20424C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659626 | |||||||
| chr4:169659665 | ACT | A | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-20382_161-2038 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169659665 | ||||||
| chr4:169659667 | T | C | 83 | a0001c0001t0033g0267 a0001c0001t0042g0256 a0001c0001t0045g0268 others(80): Show |
90 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.161-20383T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659667 | |||||||
| chr4:169659721 | A | AT | 18 | a0001c0001t0025g0004 a0001c0003t0003g0005 a0001c0003t0003g0023 others(15): Show |
20 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.161-20319dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169659721 | ||||||
| chr4:169659791 | T | A | 1 | a0001c0003t0003g0039 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.161-20259T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169659791 | |||||||
| chr4:169660075 | G | A | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-19975G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169660075 | |||||||
| chr4:169660419 | G | A | 255 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(252): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.161-19631G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169660419 | |||||||
| chr4:169660441 | T | C | 6 | a0001c0001t0005g0017 a0001c0001t0005g0238 a0001c0001t0005g0239 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-19609T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169660441 | |||||||
| chr4:169660476 | T | G | 1 | a0001c0001t0005g0236 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.161-19574T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169660476 | |||||||
| chr4:169660497 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.161-19553C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169660497 | |||||||
| chr4:169660573 | G | T | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-19477G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169660573 | |||||||
| chr4:169661078 | AAAT | A | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-18967_161-1896 others(7): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169661078 | ||||||
| chr4:169661095 | G | A | 1 | a0001c0007t0001g0158 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.161-18955G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169661095 | |||||||
| chr4:169661213 | T | C | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-18837T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169661213 | |||||||
| chr4:169661317 | A | G | 5 | a0001c0002t0002g0067 a0001c0002t0002g0084 a0001c0002t0002g0085 others(2): Show |
5 | HG01192.hp2 HG01243.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-18733A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169661317 | |||||||
| chr4:169661398 | T | G | 3 | a0001c0003t0003g0023 a0001c0003t0003g0033 a0001c0003t0003g0034 |
3 | NA18982.hp1 NA18984.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.161-18652T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169661398 | |||||||
| chr4:169661493 | A | G | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-18557A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169661493 | |||||||
| chr4:169661699 | T | C | 1 | a0001c0002t0002g0078 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.161-18351T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169661699 | |||||||
| chr4:169661774 | C | T | 1 | a0001c0003t0004g0059 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.161-18276C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169661774 | |||||||
| chr4:169661837 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.161-18213A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169661837 | |||||||
| chr4:169661838 | T | C | 1 | a0001c0003t0003g0265 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161-18212T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169661838 | |||||||
| chr4:169662006 | G | A | 58 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(55): Show |
60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.161-18044G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169662006 | |||||||
| chr4:169662208 | T | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0117 a0001c0001t0001g0135 others(1): Show |
4 | HG00544.hp2 HG01071.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-17842T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169662208 | |||||||
| chr4:169662231 | A | G | 1 | a0001c0001t0052g0040 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.161-17819A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169662231 | |||||||
| chr4:169662435 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.161-17615A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169662435 | |||||||
| chr4:169662514 | A | T | 50 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(47): Show |
56 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.161-17536A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169662514 | |||||||
| chr4:169662711 | C | T | 3 | a0001c0001t0012g0250 a0001c0001t0012g0252 a0002c0005t0012g0251 |
3 | HG03540.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.161-17339C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169662711 | |||||||
| chr4:169662854 | G | A | 1 | a0001c0003t0003g0265 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161-17196G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169662854 | |||||||
| chr4:169663125 | ATG | A | 188 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(185): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.161-16901_161-1690 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663125 | ||||||
| chr4:169663125 | ATGTG | A | 2 | a0001c0001t0005g0236 a0001c0001t0025g0004 |
3 | HG02976.hp2 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.161-16903_161-1690 others(8): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663125 | ||||||
| chr4:169663129 | GTGTGTGT others(21): Show |
G | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-16908_161-1688 others(32): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663129 | ||||||
| chr4:169663131 | GTGTGTGT others(19): Show |
G | 44 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(41): Show |
47 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(44): Show |
intron_variant | MODIFIER | c.161-16906_161-1688 others(30): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663131 | ||||||
| chr4:169663133 | GTGTGTGT others(17): Show |
G | 2 | a0001c0003t0003g0032 a0001c0003t0004g0044 |
2 | HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.161-16904_161-1688 others(28): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663133 | ||||||
| chr4:169663149 | G | A | 9 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(6): Show |
9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.161-16901G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663149 | |||||||
| chr4:169663149 | GTA | G | 5 | a0001c0001t0001g0146 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
6 | HG01257.hp1 HG01258.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-16893_161-1689 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663149 | ||||||
| chr4:169663171 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.161-16879G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663171 | |||||||
| chr4:169663179 | G | GTA | 37 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(34): Show |
37 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.161-16858_161-1685 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663179 | ||||||
| chr4:169663192 | T | A | 5 | a0001c0003t0004g0047 a0001c0003t0004g0049 a0001c0003t0004g0051 others(2): Show |
5 | HG01175.hp2 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-16858T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663192 | |||||||
| chr4:169663194 | C | T | 2 | a0001c0003t0020g0179 a0001c0003t0020g0180 |
2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.161-16856C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663194 | |||||||
| chr4:169663196 | T | C | 2 | a0001c0003t0020g0179 a0001c0003t0020g0180 |
2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.161-16854T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663196 | |||||||
| chr4:169663198 | TAC | T | 20 | a0001c0003t0004g0006 a0001c0003t0004g0043 a0001c0003t0004g0044 others(17): Show |
21 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.161-16844_161-1684 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663198 | ||||||
| chr4:169663200 | C | T | 2 | a0001c0003t0020g0179 a0001c0003t0020g0180 |
2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.161-16850C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663200 | |||||||
| chr4:169663214 | A | G | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-16836A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663214 | |||||||
| chr4:169663310 | T | G | 22 | a0001c0003t0004g0006 a0001c0003t0004g0043 a0001c0003t0004g0044 others(19): Show |
23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-16740T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663310 | |||||||
| chr4:169663311 | TTTTTTG | T | 3 | a0001c0001t0024g0210 a0001c0001t0033g0267 a0001c0001t0045g0268 |
3 | HG03579.hp2 HG03831.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.161-16736_161-1673 others(10): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663311 | ||||||
| chr4:169663314 | T | G | 1 | a0001c0001t0006g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.161-16736T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663314 | |||||||
| chr4:169663314 | TTTGTTG | T | 187 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(184): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.161-16709_161-1670 others(10): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663314 | ||||||
| chr4:169663315 | TTGTTG | T | 21 | a0001c0002t0008g0196 a0001c0003t0004g0006 a0001c0003t0004g0043 others(18): Show |
22 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.161-16733_161-1672 others(9): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663315 | ||||||
| chr4:169663316 | TGTTGTTG | T | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-16733_161-1672 others(11): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663316 | |||||||
| chr4:169663317 | G | T | 4 | a0001c0001t0005g0017 a0001c0001t0006g0189 a0001c0001t0006g0190 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-16733G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663317 | |||||||
| chr4:169663323 | G | T | 75 | a0001c0001t0001g0157 a0001c0001t0012g0250 a0001c0001t0012g0252 others(72): Show |
81 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.161-16727G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663323 | |||||||
| chr4:169663326 | G | T | 11 | a0001c0002t0008g0196 a0001c0002t0008g0197 a0001c0002t0008g0198 others(8): Show |
12 | HG02280.hp1 HG02809.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.161-16724G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663326 | |||||||
| chr4:169663408 | A | C | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-16642A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663408 | |||||||
| chr4:169663441 | C | T | 1 | a0001c0001t0006g0194 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161-16609C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663441 | |||||||
| chr4:169663452 | C | T | 1 | a0001c0001t0014g0226 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.161-16598C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663452 | |||||||
| chr4:169663474 | C | T | 3 | a0001c0002t0002g0063 a0001c0002t0002g0071 a0001c0002t0002g0072 |
3 | HG01978.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.161-16576C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663474 | |||||||
| chr4:169663510 | A | AT | 24 | a0001c0001t0007g0204 a0001c0003t0003g0003 a0001c0003t0003g0005 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-16526dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169663510 | ||||||
| chr4:169663552 | C | G | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.161-16498C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663552 | |||||||
| chr4:169663622 | G | A | 2 | a0001c0001t0001g0261 a0001c0001t0001g0264 |
2 | HG02622.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.161-16428G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663622 | |||||||
| chr4:169663637 | G | C | 1 | a0001c0001t0045g0268 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.161-16413G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663637 | |||||||
| chr4:169663729 | G | A | 60 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(57): Show |
66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.161-16321G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663729 | |||||||
| chr4:169663992 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0117 a0001c0001t0001g0135 others(1): Show |
4 | HG00544.hp2 HG01071.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-16058G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169663992 | |||||||
| chr4:169664022 | A | G | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.161-16028A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169664022 | |||||||
| chr4:169664064 | G | T | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-15986G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169664064 | |||||||
| chr4:169664215 | T | A | 1 | a0001c0001t0001g0137 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.161-15835T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169664215 | |||||||
| chr4:169664301 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.161-15749C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169664301 | |||||||
| chr4:169664349 | A | G | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-15701A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169664349 | |||||||
| chr4:169664355 | A | G | 33 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(30): Show |
33 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.161-15695A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169664355 | |||||||
| chr4:169664408 | A | G | 22 | a0001c0003t0004g0006 a0001c0003t0004g0043 a0001c0003t0004g0044 others(19): Show |
23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-15642A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169664408 | |||||||
| chr4:169664435 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.161-15615T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169664435 | |||||||
| chr4:169664888 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.161-15162G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169664888 | |||||||
| chr4:169665356 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.161-14694A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169665356 | |||||||
| chr4:169665603 | GA | G | 146 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(143): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.161-14436delA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169665603 | ||||||
| chr4:169665642 | A | G | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.161-14408A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169665642 | |||||||
| chr4:169665868 | G | A | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-14182G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169665868 | |||||||
| chr4:169665960 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.161-14090G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169665960 | |||||||
| chr4:169665980 | G | GT | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.161-14057dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169665980 | ||||||
| chr4:169665980 | G | T | 60 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(57): Show |
65 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.161-14070G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169665980 | |||||||
| chr4:169666097 | G | A | 33 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(30): Show |
33 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.161-13953G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169666097 | |||||||
| chr4:169666206 | C | G | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-13844C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169666206 | |||||||
| chr4:169666257 | A | G | 2 | a0001c0003t0003g0257 a0001c0003t0003g0259 |
2 | HG03704.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.161-13793A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169666257 | |||||||
| chr4:169666267 | A | G | 22 | a0001c0003t0004g0006 a0001c0003t0004g0043 a0001c0003t0004g0044 others(19): Show |
23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-13783A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169666267 | |||||||
| chr4:169666503 | A | G | 6 | a0001c0001t0005g0017 a0001c0001t0005g0238 a0001c0001t0005g0239 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-13547A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169666503 | |||||||
| chr4:169666994 | G | T | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.161-13056G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169666994 | |||||||
| chr4:169667144 | G | T | 1 | a0001c0001t0028g0213 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.161-12906G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667144 | |||||||
| chr4:169667296 | CT | C | 27 | a0001c0001t0012g0250 a0001c0001t0012g0252 a0001c0003t0003g0003 others(24): Show |
29 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(26): Show |
intron_variant | MODIFIER | c.161-12744delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169667296 | ||||||
| chr4:169667316 | C | T | 1 | a0001c0002t0009g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.161-12734C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667316 | |||||||
| chr4:169667433 | A | G | 1 | a0001c0001t0035g0024 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.161-12617A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667433 | |||||||
| chr4:169667465 | T | C | 1 | a0001c0001t0048g0217 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.161-12585T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667465 | |||||||
| chr4:169667521 | A | G | 1 | a0001c0003t0003g0265 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161-12529A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667521 | |||||||
| chr4:169667680 | T | TAAAAATA others(309): Show |
20 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(17): Show |
20 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.161-12352_161-1235 others(320): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169667680 | ||||||
| chr4:169667680 | T | TAAAAATA others(310): Show |
5 | a0001c0001t0016g0218 a0001c0001t0024g0210 a0001c0001t0024g0214 others(2): Show |
5 | HG02896.hp1 HG03688.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-12352_161-1235 others(321): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169667680 | ||||||
| chr4:169667680 | T | TAAAAATA others(309): Show |
8 | a0001c0001t0010g0228 a0001c0001t0010g0230 a0001c0001t0013g0225 others(5): Show |
8 | HG00738.hp1 HG01168.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-12352_161-1235 others(320): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169667680 | ||||||
| chr4:169667680 | T | TAAAAATA others(310): Show |
1 | a0001c0001t0014g0221 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.161-12352_161-1235 others(321): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169667680 | ||||||
| chr4:169667690 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.161-12360G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667690 | |||||||
| chr4:169667753 | C | CT | 10 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(7): Show |
10 | HG00609.hp1 HG01884.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-12286dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169667753 | ||||||
| chr4:169667776 | C | T | 1 | a0001c0001t0010g0216 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.161-12274C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667776 | |||||||
| chr4:169667907 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.161-12143G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667907 | |||||||
| chr4:169667927 | G | C | 9 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(6): Show |
9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.161-12123G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667927 | |||||||
| chr4:169667985 | T | C | 143 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(140): Show |
152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.161-12065T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169667985 | |||||||
| chr4:169668043 | A | AT | 84 | a0001c0001t0001g0114 a0001c0001t0001g0125 a0001c0001t0001g0127 others(81): Show |
91 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.161-11984dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169668043 | ||||||
| chr4:169668043 | A | ATT | 25 | a0001c0001t0012g0252 a0001c0002t0002g0066 a0001c0002t0002g0070 others(22): Show |
27 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.161-11985_161-1198 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169668043 | ||||||
| chr4:169668043 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0141 |
3 | HG01346.hp2 HG01433.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.161-12007A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169668043 | |||||||
| chr4:169668043 | A | T | 2 | a0001c0001t0001g0123 a0001c0003t0003g0265 |
2 | HG03139.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.161-12007A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169668043 | |||||||
| chr4:169668046 | T | TG | 30 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(27): Show |
30 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.161-12004_161-1200 others(5): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169668046 | |||||||
| chr4:169668047 | T | G | 1 | a0001c0001t0052g0040 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.161-12003T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169668047 | |||||||
| chr4:169668166 | GGTT | G | 60 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(57): Show |
66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.161-11880_161-1187 others(7): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169668166 | ||||||
| chr4:169668214 | C | T | 1 | a0001c0001t0011g0185 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.161-11836C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169668214 | |||||||
| chr4:169668474 | A | G | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-11576A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169668474 | |||||||
| chr4:169668523 | C | T | 16 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(13): Show |
17 | HG01884.hp1 HG02572.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.161-11527C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169668523 | |||||||
| chr4:169668616 | G | A | 1 | a0001c0001t0035g0024 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.161-11434G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169668616 | |||||||
| chr4:169668730 | A | AT | 7 | a0001c0001t0001g0137 a0001c0001t0001g0254 a0001c0001t0010g0230 others(4): Show |
7 | HG01168.hp2 HG02896.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-11305dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169668730 | ||||||
| chr4:169668730 | A | ATT | 32 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(29): Show |
32 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.161-11306_161-1130 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169668730 | ||||||
| chr4:169668730 | AT | A | 29 | a0001c0001t0001g0124 a0001c0001t0005g0236 a0001c0001t0005g0242 others(26): Show |
30 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(27): Show |
intron_variant | MODIFIER | c.161-11305delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169668730 | ||||||
| chr4:169668928 | G | A | 1 | a0001c0002t0002g0092 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.161-11122G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169668928 | |||||||
| chr4:169669080 | G | C | 1 | a0001c0003t0004g0058 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.161-10970G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169669080 | |||||||
| chr4:169669238 | A | G | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.161-10812A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169669238 | |||||||
| chr4:169669240 | C | T | 1 | a0001c0003t0003g0005 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.161-10810C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169669240 | |||||||
| chr4:169669789 | G | A | 46 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(43): Show |
49 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.161-10261G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169669789 | |||||||
| chr4:169669832 | C | T | 6 | a0001c0001t0011g0185 a0001c0001t0011g0186 a0001c0001t0011g0187 others(3): Show |
7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-10218C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169669832 | |||||||
| chr4:169669838 | A | G | 46 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(43): Show |
49 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.161-10212A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169669838 | |||||||
| chr4:169669843 | A | G | 2 | a0001c0002t0002g0007 a0001c0002t0002g0066 |
3 | NA18947.hp2 NA18981.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.161-10207A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169669843 | |||||||
| chr4:169670328 | G | A | 7 | a0001c0003t0004g0006 a0001c0003t0004g0054 a0001c0003t0004g0056 others(4): Show |
8 | HG00639.hp2 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.161-9722G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670328 | |||||||
| chr4:169670384 | A | G | 1 | a0001c0001t0052g0040 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.161-9666A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670384 | |||||||
| chr4:169670464 | C | T | 22 | a0001c0003t0004g0006 a0001c0003t0004g0043 a0001c0003t0004g0044 others(19): Show |
23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-9586C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670464 | |||||||
| chr4:169670491 | C | T | 1 | a0001c0001t0052g0040 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.161-9559C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670491 | |||||||
| chr4:169670494 | T | G | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-9556T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670494 | |||||||
| chr4:169670556 | C | T | 1 | a0001c0001t0025g0004 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.161-9494C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670556 | |||||||
| chr4:169670595 | C | T | 1 | a0001c0003t0004g0049 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.161-9455C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670595 | |||||||
| chr4:169670701 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.161-9349C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670701 | |||||||
| chr4:169670781 | C | G | 1 | a0001c0001t0012g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.161-9269C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670781 | |||||||
| chr4:169670871 | A | C | 6 | a0001c0001t0011g0185 a0001c0001t0011g0186 a0001c0001t0011g0187 others(3): Show |
7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-9179A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169670871 | |||||||
| chr4:169671147 | C | T | 6 | a0001c0001t0011g0185 a0001c0001t0011g0186 a0001c0001t0011g0187 others(3): Show |
7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-8903C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169671147 | |||||||
| chr4:169671303 | T | A | 60 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(57): Show |
66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.161-8747T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169671303 | |||||||
| chr4:169671489 | A | G | 2 | a0001c0001t0015g0015 a0001c0001t0015g0184 |
3 | HG02615.hp2 HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.161-8561A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169671489 | |||||||
| chr4:169671583 | C | A | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-8467C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169671583 | |||||||
| chr4:169671759 | G | T | 1 | a0001c0001t0007g0204 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.161-8291G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169671759 | |||||||
| chr4:169671866 | G | T | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-8184G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169671866 | |||||||
| chr4:169671994 | G | A | 60 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(57): Show |
66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.161-8056G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169671994 | |||||||
| chr4:169672069 | G | A | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-7981G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672069 | |||||||
| chr4:169672073 | G | A | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-7977G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672073 | |||||||
| chr4:169672076 | G | T | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-7974G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672076 | |||||||
| chr4:169672169 | G | A | 3 | a0001c0003t0003g0026 a0001c0003t0003g0027 a0001c0003t0003g0028 |
3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.161-7881G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672169 | |||||||
| chr4:169672169 | G | T | 1 | a0001c0001t0007g0204 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.161-7881G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672169 | |||||||
| chr4:169672218 | A | G | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-7832A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672218 | |||||||
| chr4:169672220 | T | TA | 6 | a0001c0003t0003g0031 a0001c0003t0003g0257 a0001c0003t0003g0259 others(3): Show |
6 | HG01358.hp1 HG03516.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-7830_161-7829i others(3): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672220 | |||||||
| chr4:169672220 | T | TAGATA | 13 | a0001c0003t0003g0003 a0001c0003t0003g0023 a0001c0003t0003g0026 others(10): Show |
14 | HG02723.hp2 HG02886.hp2 HG02896.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-7830_161-7829i others(7): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672220 | |||||||
| chr4:169672220 | T | TAGATAGA others(2): Show |
14 | a0001c0003t0003g0005 a0001c0003t0003g0027 a0001c0003t0003g0029 others(11): Show |
15 | HG01516.hp2 HG01517.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.161-7830_161-7829i others(11): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672220 | |||||||
| chr4:169672220 | T | TAGATAGA others(6): Show |
12 | a0001c0003t0003g0028 a0001c0003t0003g0030 a0001c0003t0004g0006 others(9): Show |
12 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.161-7830_161-7829i others(15): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672220 | |||||||
| chr4:169672220 | T | TAGATAGA others(10): Show |
1 | a0001c0003t0003g0037 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.161-7830_161-7829i others(19): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672220 | |||||||
| chr4:169672220 | T | TGATA | 22 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(19): Show |
23 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.161-7793_161-7790d others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169672220 | ||||||
| chr4:169672220 | T | TGATAGAT others(1): Show |
42 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(39): Show |
44 | HG00544.hp1 HG00558.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.161-7797_161-7790d others(10): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169672220 | ||||||
| chr4:169672220 | T | TGATAGAT others(5): Show |
118 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(115): Show |
120 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.161-7801_161-7790d others(14): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169672220 | ||||||
| chr4:169672220 | T | TGATAGAT others(9): Show |
29 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0127 others(26): Show |
29 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.161-7805_161-7790d others(18): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169672220 | ||||||
| chr4:169672220 | T | TGATAGAT others(13): Show |
13 | a0001c0001t0001g0130 a0001c0001t0011g0185 a0001c0001t0011g0187 others(10): Show |
13 | HG00140.hp2 HG00609.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.161-7809_161-7790d others(22): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169672220 | ||||||
| chr4:169672220 | T | TGATAGAT others(17): Show |
2 | a0001c0001t0014g0221 a0001c0002t0002g0103 |
2 | HG01099.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.161-7813_161-7790d others(26): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169672220 | ||||||
| chr4:169672431 | C | T | 33 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(30): Show |
33 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.161-7619C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672431 | |||||||
| chr4:169672549 | T | G | 1 | a0001c0001t0001g0122 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.161-7501T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672549 | |||||||
| chr4:169672653 | TTTTGTTT others(5): Show |
T | 1 | a0001c0001t0001g0182 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.161-7385_161-7374d others(14): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169672653 | ||||||
| chr4:169672802 | T | C | 6 | a0001c0001t0011g0185 a0001c0001t0011g0186 a0001c0001t0011g0187 others(3): Show |
7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-7248T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672802 | |||||||
| chr4:169672820 | C | T | 2 | a0001c0001t0015g0015 a0001c0001t0015g0184 |
3 | HG02615.hp2 HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.161-7230C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672820 | |||||||
| chr4:169672821 | G | A | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-7229G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672821 | |||||||
| chr4:169672895 | C | T | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.161-7155C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672895 | |||||||
| chr4:169672907 | T | C | 260 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(257): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.161-7143T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169672907 | |||||||
| chr4:169673044 | T | C | 254 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(251): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.161-7006T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169673044 | |||||||
| chr4:169673109 | C | T | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-6941C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169673109 | |||||||
| chr4:169673152 | T | C | 4 | a0001c0003t0003g0026 a0001c0003t0003g0027 a0001c0003t0003g0028 others(1): Show |
4 | HG02055.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-6898T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169673152 | |||||||
| chr4:169673177 | A | G | 238 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(235): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.161-6873A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169673177 | |||||||
| chr4:169673433 | C | T | 7 | a0001c0001t0011g0185 a0001c0001t0011g0186 a0001c0001t0011g0187 others(4): Show |
8 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-6617C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169673433 | |||||||
| chr4:169673486 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.161-6564C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169673486 | |||||||
| chr4:169673741 | A | G | 60 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(57): Show |
66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.161-6309A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169673741 | |||||||
| chr4:169673766 | T | G | 1 | a0001c0001t0001g0010 | 2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.161-6284T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169673766 | |||||||
| chr4:169674040 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG00544.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.161-6010A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674040 | |||||||
| chr4:169674041 | T | C | 2 | a0001c0001t0015g0015 a0001c0001t0015g0184 |
3 | HG02615.hp2 HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.161-6009T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674041 | |||||||
| chr4:169674262 | G | A | 13 | a0001c0003t0003g0005 a0001c0003t0003g0023 a0001c0003t0003g0029 others(10): Show |
14 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.161-5788G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674262 | |||||||
| chr4:169674297 | G | C | 3 | a0001c0003t0003g0023 a0001c0003t0003g0033 a0001c0003t0003g0034 |
3 | NA18982.hp1 NA18984.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.161-5753G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674297 | |||||||
| chr4:169674360 | G | C | 1 | a0001c0003t0023g0045 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.161-5690G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674360 | |||||||
| chr4:169674483 | T | G | 260 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(257): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.161-5567T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674483 | |||||||
| chr4:169674652 | A | G | 60 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(57): Show |
66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.161-5398A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674652 | |||||||
| chr4:169674653 | A | T | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.161-5397A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674653 | |||||||
| chr4:169674774 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.161-5276C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674774 | |||||||
| chr4:169674931 | G | A | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-5119G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674931 | |||||||
| chr4:169674971 | C | A | 238 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(235): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.161-5079C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169674971 | |||||||
| chr4:169675021 | C | T | 2 | a0001c0001t0025g0004 a0001c0001t0034g0233 |
3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.161-5029C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169675021 | |||||||
| chr4:169675132 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.161-4918G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169675132 | |||||||
| chr4:169675266 | T | A | 1 | a0001c0001t0001g0156 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.161-4784T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169675266 | |||||||
| chr4:169675429 | G | C | 5 | a0001c0001t0005g0236 a0001c0001t0005g0242 a0001c0001t0005g0243 others(2): Show |
5 | HG02055.hp1 HG02258.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-4621G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169675429 | |||||||
| chr4:169675486 | A | G | 1 | a0001c0001t0014g0226 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.161-4564A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169675486 | |||||||
| chr4:169675528 | C | T | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-4522C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169675528 | |||||||
| chr4:169675877 | A | G | 61 | a0001c0001t0001g0153 a0001c0002t0002g0001 a0001c0002t0002g0002 others(58): Show |
67 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.161-4173A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169675877 | |||||||
| chr4:169675902 | G | A | 1 | a0001c0001t0001g0010 | 2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.161-4148G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169675902 | |||||||
| chr4:169675942 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.161-4108A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169675942 | |||||||
| chr4:169676162 | C | A | 1 | a0001c0001t0001g0262 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.161-3888C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169676162 | |||||||
| chr4:169676280 | A | T | 260 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(257): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.161-3770A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169676280 | |||||||
| chr4:169676420 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.161-3630C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169676420 | |||||||
| chr4:169676512 | C | CT | 60 | a0001c0001t0042g0256 a0001c0002t0002g0001 a0001c0002t0002g0002 others(57): Show |
66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.161-3527dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169676512 | ||||||
| chr4:169676512 | CT | C | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.161-3527delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169676512 | ||||||
| chr4:169676569 | C | T | 2 | a0001c0003t0020g0179 a0001c0003t0020g0180 |
2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.161-3481C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169676569 | |||||||
| chr4:169676650 | A | AT | 8 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0001g0160 others(5): Show |
8 | HG01175.hp1 HG02738.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.161-3381dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169676650 | ||||||
| chr4:169676650 | AT | A | 55 | a0001c0001t0001g0115 a0001c0001t0001g0128 a0001c0001t0001g0130 others(52): Show |
59 | HG00639.hp2 HG01175.hp2 HG01192.hp2 others(56): Show |
intron_variant | MODIFIER | c.161-3381delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169676650 | ||||||
| chr4:169676650 | ATT | A | 57 | a0001c0001t0042g0256 a0001c0002t0002g0001 a0001c0002t0002g0002 others(54): Show |
63 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.161-3382_161-3381d others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169676650 | ||||||
| chr4:169676670 | G | C | 1 | a0001c0001t0045g0268 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.161-3380G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169676670 | |||||||
| chr4:169676821 | A | G | 1 | a0001c0003t0037g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.161-3229A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169676821 | |||||||
| chr4:169676873 | T | C | 1 | a0001c0001t0034g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.161-3177T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169676873 | |||||||
| chr4:169676997 | G | A | 51 | a0001c0002t0002g0001 a0001c0002t0002g0064 a0001c0002t0002g0070 others(48): Show |
56 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(53): Show |
intron_variant | MODIFIER | c.161-3053G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169676997 | |||||||
| chr4:169677311 | C | T | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-2739C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169677311 | |||||||
| chr4:169677431 | T | G | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-2619T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169677431 | |||||||
| chr4:169677590 | A | C | 1 | a0001c0002t0008g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.161-2460A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169677590 | |||||||
| chr4:169677622 | A | G | 12 | a0001c0003t0003g0005 a0001c0003t0003g0023 a0001c0003t0003g0029 others(9): Show |
13 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.161-2428A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169677622 | |||||||
| chr4:169677695 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.161-2355C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169677695 | |||||||
| chr4:169677835 | C | G | 254 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(251): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.161-2215C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169677835 | |||||||
| chr4:169677894 | CT | C | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-2151delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169677894 | ||||||
| chr4:169678280 | C | A | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.161-1770C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678280 | |||||||
| chr4:169678420 | T | A | 1 | a0001c0001t0014g0226 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.161-1630T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678420 | |||||||
| chr4:169678558 | C | T | 1 | a0001c0003t0003g0038 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.161-1492C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678558 | |||||||
| chr4:169678813 | C | T | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-1237C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678813 | |||||||
| chr4:169678860 | T | C | 1 | a0001c0001t0043g0248 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161-1190T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678860 | |||||||
| chr4:169678861 | A | C | 1 | a0001c0001t0043g0248 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161-1189A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678861 | |||||||
| chr4:169678869 | T | C | 1 | a0001c0001t0043g0248 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161-1181T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678869 | |||||||
| chr4:169678878 | T | C | 1 | a0001c0001t0043g0248 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161-1172T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678878 | |||||||
| chr4:169678879 | G | C | 1 | a0001c0001t0043g0248 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161-1171G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678879 | |||||||
| chr4:169678887 | T | C | 1 | a0001c0001t0043g0248 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161-1163T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678887 | |||||||
| chr4:169678893 | C | T | 1 | a0001c0001t0043g0248 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161-1157C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678893 | |||||||
| chr4:169678894 | C | G | 1 | a0001c0001t0043g0248 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161-1156C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678894 | |||||||
| chr4:169678898 | C | T | 1 | a0001c0001t0043g0248 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.161-1152C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678898 | |||||||
| chr4:169678987 | GCCGGGCG others(17): Show |
G | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-1060_161-1037d others(26): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169678987 | ||||||
| chr4:169678989 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.161-1061C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678989 | |||||||
| chr4:169678993 | C | A | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.161-1057C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169678993 | |||||||
| chr4:169679070 | C | T | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-980C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679070 | |||||||
| chr4:169679076 | C | A | 9 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(6): Show |
9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.161-974C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679076 | |||||||
| chr4:169679085 | C | T | 1 | a0001c0001t0012g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.161-965C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679085 | |||||||
| chr4:169679124 | A | G | 3 | a0001c0003t0004g0044 a0001c0003t0004g0046 a0001c0003t0023g0045 |
3 | HG02486.hp1 HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.161-926A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679124 | |||||||
| chr4:169679140 | C | T | 1 | a0001c0003t0003g0036 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.161-910C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679140 | |||||||
| chr4:169679141 | G | C | 1 | a0001c0003t0003g0036 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.161-909G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679141 | |||||||
| chr4:169679152 | G | C | 1 | a0001c0001t0006g0194 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161-898G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679152 | |||||||
| chr4:169679181 | G | A | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.161-869G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679181 | |||||||
| chr4:169679182 | C | T | 1 | a0001c0002t0002g0104 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.161-868C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679182 | |||||||
| chr4:169679253 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.161-797G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679253 | |||||||
| chr4:169679310 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.161-740G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679310 | |||||||
| chr4:169679318 | C | T | 33 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(30): Show |
33 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.161-732C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679318 | |||||||
| chr4:169679327 | C | CGGGATGG others(33): Show |
4 | a0001c0001t0001g0011 a0001c0001t0001g0134 a0001c0001t0001g0137 others(1): Show |
5 | HG02129.hp1 NA18747.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-711_161-672dup others(40): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169679327 | ||||||
| chr4:169679335 | C | T | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-715C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679335 | |||||||
| chr4:169679387 | G | A | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.161-663G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679387 | |||||||
| chr4:169679483 | C | CG | 7 | a0001c0001t0001g0155 a0001c0001t0005g0241 a0001c0001t0010g0208 others(4): Show |
7 | HG01109.hp1 HG01255.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-563dupG | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169679483 | ||||||
| chr4:169679496 | G | A | 1 | a0001c0002t0002g0080 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.161-554G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679496 | |||||||
| chr4:169679565 | G | C | 1 | a0001c0003t0003g0039 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.161-485G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679565 | |||||||
| chr4:169679654 | C | T | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.161-396C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679654 | |||||||
| chr4:169679672 | C | G | 7 | a0001c0003t0003g0003 a0001c0003t0003g0257 a0001c0003t0003g0259 others(4): Show |
8 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-378C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679672 | |||||||
| chr4:169679681 | G | T | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.161-369G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679681 | |||||||
| chr4:169679772 | C | G | 1 | a0001c0001t0001g0134 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.161-278C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679772 | |||||||
| chr4:169679782 | C | T | 1 | a0001c0002t0009g0100 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.161-268C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679782 | |||||||
| chr4:169679783 | G | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.161-267G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679783 | |||||||
| chr4:169679835 | C | T | 1 | a0001c0003t0040g0266 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.161-215C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679835 | |||||||
| chr4:169679863 | AGGGAGAC others(33): Show |
A | 55 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(52): Show |
61 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.161-172_161-133del others(40): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 169679863 | ||||||
| chr4:169679887 | C | T | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-163C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679887 | |||||||
| chr4:169679893 | C | T | 1 | a0001c0003t0003g0265 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161-157C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169679893 | |||||||
| chr4:169680021 | A | G | 33 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(30): Show |
33 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.161-29A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 2/12 | chr4 | 169680021 | |||||||
| chr4:169680298 | T | C | 50 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(47): Show |
56 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.318+91T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169680298 | |||||||
| chr4:169680507 | A | G | 3 | a0001c0001t0007g0220 a0001c0001t0007g0227 a0001c0001t0028g0213 |
3 | HG00140.hp1 HG01109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.318+300A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169680507 | |||||||
| chr4:169680672 | C | T | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.318+465C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169680672 | |||||||
| chr4:169680757 | G | C | 1 | a0001c0001t0047g0202 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.318+550G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169680757 | |||||||
| chr4:169680777 | A | C | 1 | a0001c0003t0003g0039 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.318+570A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169680777 | |||||||
| chr4:169680804 | C | T | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.318+597C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169680804 | |||||||
| chr4:169680821 | A | G | 248 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(245): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.318+614A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169680821 | |||||||
| chr4:169680835 | A | G | 8 | a0001c0003t0004g0006 a0001c0003t0004g0043 a0001c0003t0004g0054 others(5): Show |
9 | HG00639.hp2 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.318+628A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169680835 | |||||||
| chr4:169680924 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0167 |
2 | HG01074.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.318+717C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169680924 | |||||||
| chr4:169681031 | C | A | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.318+824C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681031 | |||||||
| chr4:169681045 | C | T | 2 | a0001c0001t0025g0004 a0001c0001t0034g0233 |
3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.318+838C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681045 | |||||||
| chr4:169681072 | C | T | 60 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(57): Show |
62 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.318+865C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681072 | |||||||
| chr4:169681073 | G | A | 60 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(57): Show |
66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.318+866G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681073 | |||||||
| chr4:169681116 | T | G | 1 | a0001c0001t0001g0129 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.318+909T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681116 | |||||||
| chr4:169681245 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.318+1038G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681245 | |||||||
| chr4:169681273 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0129 |
2 | HG00280.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.318+1066C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681273 | |||||||
| chr4:169681347 | C | T | 4 | a0001c0003t0003g0026 a0001c0003t0003g0027 a0001c0003t0003g0028 others(1): Show |
4 | HG02055.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+1140C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681347 | |||||||
| chr4:169681348 | A | G | 60 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(57): Show |
66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.318+1141A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681348 | |||||||
| chr4:169681416 | T | G | 3 | a0001c0001t0001g0115 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | NA19068.hp2 NA19078.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.318+1209T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681416 | |||||||
| chr4:169681573 | A | G | 1 | a0001c0001t0016g0203 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.318+1366A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681573 | |||||||
| chr4:169681706 | T | A | 25 | a0001c0001t0025g0004 a0001c0003t0003g0003 a0001c0003t0003g0005 others(22): Show |
28 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.318+1499T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169681706 | |||||||
| chr4:169682038 | G | A | 254 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(251): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.318+1831G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169682038 | |||||||
| chr4:169682215 | TATATA | T | 3 | a0001c0001t0033g0267 a0001c0001t0045g0268 a0001c0003t0003g0265 |
3 | HG03139.hp1 HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.318+2017_318+2021d others(7): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 169682215 | ||||||
| chr4:169682255 | A | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0121 a0001c0001t0001g0149 others(3): Show |
6 | HG01099.hp2 HG01258.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.318+2048A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169682255 | |||||||
| chr4:169682291 | A | G | 5 | a0001c0002t0002g0067 a0001c0002t0002g0084 a0001c0002t0002g0085 others(2): Show |
5 | HG01192.hp2 HG01243.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+2084A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169682291 | |||||||
| chr4:169682368 | A | G | 7 | a0001c0001t0011g0185 a0001c0001t0011g0186 a0001c0001t0011g0187 others(4): Show |
8 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.318+2161A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169682368 | |||||||
| chr4:169682372 | T | C | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.318+2165T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169682372 | |||||||
| chr4:169682485 | C | G | 2 | a0001c0001t0025g0004 a0001c0001t0034g0233 |
3 | HG02976.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.318+2278C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169682485 | |||||||
| chr4:169682550 | C | T | 1 | a0001c0001t0001g0010 | 2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.318+2343C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169682550 | |||||||
| chr4:169682828 | A | G | 1 | a0001c0001t0001g0116 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.318+2621A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169682828 | |||||||
| chr4:169682908 | A | G | 3 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0007t0001g0158 |
3 | HG00642.hp1 HG00733.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.318+2701A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169682908 | |||||||
| chr4:169683435 | C | T | 3 | a0001c0003t0003g0026 a0001c0003t0003g0027 a0001c0003t0003g0028 |
3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.318+3228C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169683435 | |||||||
| chr4:169683657 | A | G | 1 | a0001c0003t0003g0030 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.318+3450A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169683657 | |||||||
| chr4:169683679 | G | A | 259 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(256): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.318+3472G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169683679 | |||||||
| chr4:169683744 | A | AT | 16 | a0001c0001t0001g0135 a0001c0001t0001g0264 a0001c0001t0006g0189 others(13): Show |
17 | HG01516.hp2 HG01517.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.318+3555dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 169683744 | ||||||
| chr4:169683744 | AT | A | 7 | a0001c0001t0001g0138 a0001c0001t0001g0143 a0001c0001t0001g0146 others(4): Show |
7 | HG01257.hp2 HG02965.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.318+3555delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 169683744 | ||||||
| chr4:169683765 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.318+3558G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169683765 | |||||||
| chr4:169683772 | C | G | 7 | a0001c0001t0011g0185 a0001c0001t0011g0186 a0001c0001t0011g0187 others(4): Show |
8 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.318+3565C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169683772 | |||||||
| chr4:169683912 | T | G | 4 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0032g0181 others(1): Show |
4 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+3705T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169683912 | |||||||
| chr4:169683959 | T | G | 4 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(1): Show |
4 | HG01884.hp1 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-3699T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169683959 | |||||||
| chr4:169683971 | G | A | 11 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0006g0189 others(8): Show |
11 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.319-3687G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169683971 | |||||||
| chr4:169684266 | T | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0182 |
2 | HG00609.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.319-3392T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169684266 | |||||||
| chr4:169684387 | G | A | 60 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(57): Show |
66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.319-3271G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169684387 | |||||||
| chr4:169684561 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.319-3097T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169684561 | |||||||
| chr4:169684637 | T | C | 7 | a0001c0003t0003g0003 a0001c0003t0003g0257 a0001c0003t0003g0259 others(4): Show |
8 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.319-3021T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169684637 | |||||||
| chr4:169684814 | A | G | 2 | a0001c0001t0018g0166 a0001c0001t0018g0168 |
2 | HG00323.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.319-2844A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169684814 | |||||||
| chr4:169684826 | C | A | 1 | a0001c0001t0001g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.319-2832C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169684826 | |||||||
| chr4:169684877 | A | G | 95 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(92): Show |
101 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.319-2781A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169684877 | |||||||
| chr4:169684971 | G | C | 33 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(30): Show |
33 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.319-2687G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169684971 | |||||||
| chr4:169684975 | A | AT | 16 | a0001c0001t0005g0236 a0001c0001t0005g0243 a0001c0001t0011g0185 others(13): Show |
17 | HG02055.hp1 HG02055.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.319-2660dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 169684975 | ||||||
| chr4:169684975 | AT | A | 148 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(145): Show |
161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.319-2660delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 169684975 | ||||||
| chr4:169684975 | ATT | A | 18 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0118 others(15): Show |
18 | HG00639.hp1 HG01069.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.319-2661_319-2660d others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 169684975 | ||||||
| chr4:169684985 | T | C | 1 | a0001c0002t0002g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.319-2673T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169684985 | |||||||
| chr4:169685191 | G | T | 1 | a0001c0004t0002g0073 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.319-2467G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685191 | |||||||
| chr4:169685193 | G | A | 3 | a0001c0001t0012g0250 a0001c0001t0012g0252 a0002c0005t0012g0251 |
3 | HG03540.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.319-2465G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685193 | |||||||
| chr4:169685306 | C | T | 21 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(18): Show |
23 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.319-2352C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685306 | |||||||
| chr4:169685368 | C | A | 1 | a0001c0001t0001g0159 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.319-2290C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685368 | |||||||
| chr4:169685436 | T | C | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.319-2222T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685436 | |||||||
| chr4:169685472 | C | G | 1 | a0001c0002t0017g0150 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.319-2186C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685472 | |||||||
| chr4:169685638 | G | A | 1 | a0001c0001t0034g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.319-2020G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685638 | |||||||
| chr4:169685645 | A | G | 1 | a0001c0001t0006g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.319-2013A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685645 | |||||||
| chr4:169685675 | C | T | 5 | a0001c0003t0003g0003 a0001c0003t0003g0257 a0001c0003t0003g0259 others(2): Show |
6 | HG02896.hp2 HG02897.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-1983C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685675 | |||||||
| chr4:169685681 | A | G | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.319-1977A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685681 | |||||||
| chr4:169685780 | TATC | T | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.319-1875_319-1873d others(5): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 169685780 | ||||||
| chr4:169685925 | G | A | 50 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(47): Show |
56 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.319-1733G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685925 | |||||||
| chr4:169685987 | C | T | 2 | a0001c0003t0020g0179 a0001c0003t0020g0180 |
2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.319-1671C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169685987 | |||||||
| chr4:169686006 | G | A | 85 | a0001c0001t0033g0267 a0001c0001t0042g0256 a0001c0001t0045g0268 others(82): Show |
92 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.319-1652G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686006 | |||||||
| chr4:169686059 | A | G | 6 | a0001c0001t0011g0185 a0001c0001t0011g0186 a0001c0001t0011g0187 others(3): Show |
7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.319-1599A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686059 | |||||||
| chr4:169686251 | A | T | 1 | a0001c0003t0004g0052 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.319-1407A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686251 | |||||||
| chr4:169686269 | A | G | 1 | a0001c0001t0006g0192 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.319-1389A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686269 | |||||||
| chr4:169686419 | C | CT | 59 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(56): Show |
65 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.319-1224dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 169686419 | ||||||
| chr4:169686437 | G | T | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.319-1221G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686437 | |||||||
| chr4:169686529 | G | T | 1 | a0001c0001t0014g0224 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.319-1129G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686529 | |||||||
| chr4:169686555 | T | TA | 3 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0007t0001g0158 |
3 | HG00642.hp1 HG00733.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.319-1102dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr4 | 169686555 | ||||||
| chr4:169686565 | C | T | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.319-1093C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686565 | |||||||
| chr4:169686596 | T | C | 1 | a0001c0003t0040g0266 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.319-1062T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686596 | |||||||
| chr4:169686652 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.319-1006T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686652 | |||||||
| chr4:169686695 | G | A | 1 | a0001c0001t0016g0211 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.319-963G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686695 | |||||||
| chr4:169686882 | T | C | 46 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(43): Show |
49 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.319-776T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686882 | |||||||
| chr4:169686884 | A | G | 46 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(43): Show |
49 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.319-774A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169686884 | |||||||
| chr4:169687246 | T | A | 60 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(57): Show |
66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.319-412T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169687246 | |||||||
| chr4:169687331 | A | T | 6 | a0001c0001t0011g0185 a0001c0001t0011g0186 a0001c0001t0011g0187 others(3): Show |
7 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.319-327A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169687331 | |||||||
| chr4:169687431 | T | A | 49 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(46): Show |
55 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.319-227T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 3/12 | chr4 | 169687431 | |||||||
| chr4:169687829 | A | G | 22 | a0001c0003t0004g0006 a0001c0003t0004g0043 a0001c0003t0004g0044 others(19): Show |
23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.418+72A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169687829 | |||||||
| chr4:169687985 | G | C | 1 | a0001c0001t0012g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.418+228G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169687985 | |||||||
| chr4:169688070 | T | C | 1 | a0001c0001t0034g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.418+313T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169688070 | |||||||
| chr4:169688100 | T | C | 23 | a0001c0002t0008g0074 a0001c0003t0004g0006 a0001c0003t0004g0043 others(20): Show |
24 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.418+343T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169688100 | |||||||
| chr4:169688130 | T | C | 1 | a0001c0001t0005g0236 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.418+373T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169688130 | |||||||
| chr4:169688158 | T | G | 2 | a0001c0002t0002g0007 a0001c0002t0002g0066 |
3 | NA18947.hp2 NA18981.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.418+401T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169688158 | |||||||
| chr4:169688295 | C | T | 2 | a0001c0003t0004g0046 a0001c0003t0023g0045 |
2 | HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.418+538C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169688295 | |||||||
| chr4:169688363 | T | C | 60 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(57): Show |
66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.418+606T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169688363 | |||||||
| chr4:169688413 | A | T | 9 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(6): Show |
9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.419-630A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169688413 | |||||||
| chr4:169688568 | G | T | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.419-475G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169688568 | |||||||
| chr4:169688910 | T | G | 1 | a0001c0001t0001g0014 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.419-133T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 4/12 | chr4 | 169688910 | |||||||
| chr4:169689473 | T | C | 1 | a0001c0001t0001g0014 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.606+243T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/12 | chr4 | 169689473 | |||||||
| chr4:169689581 | A | G | 1 | a0001c0002t0002g0062 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.606+351A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/12 | chr4 | 169689581 | |||||||
| chr4:169689659 | G | A | 239 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(236): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.606+429G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/12 | chr4 | 169689659 | |||||||
| chr4:169689724 | A | G | 60 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(57): Show |
66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.606+494A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/12 | chr4 | 169689724 | |||||||
| chr4:169689728 | T | C | 1 | a0001c0003t0004g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.606+498T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/12 | chr4 | 169689728 | |||||||
| chr4:169690137 | C | CT | 227 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(224): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.607-374dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 169690137 | ||||||
| chr4:169690137 | C | CTT | 19 | a0001c0001t0001g0253 a0001c0001t0006g0189 a0001c0001t0006g0190 others(16): Show |
20 | HG01884.hp1 HG01981.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.607-375_607-374dup others(2): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 169690137 | ||||||
| chr4:169690370 | T | C | 7 | a0001c0003t0003g0003 a0001c0003t0003g0257 a0001c0003t0003g0259 others(4): Show |
8 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.607-160T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/12 | chr4 | 169690370 | |||||||
| chr4:169690391 | C | G | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.607-139C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 5/12 | chr4 | 169690391 | |||||||
| chr4:169690719 | A | G | 1 | a0001c0003t0003g0029 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.729+67A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169690719 | |||||||
| chr4:169690739 | G | A | 1 | a0001c0001t0012g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.729+87G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169690739 | |||||||
| chr4:169690777 | T | A | 1 | a0001c0001t0034g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.729+125T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169690777 | |||||||
| chr4:169690830 | A | G | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.729+178A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169690830 | |||||||
| chr4:169690928 | C | A | 1 | a0001c0001t0001g0022 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.729+276C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169690928 | |||||||
| chr4:169691012 | T | TG | 5 | a0001c0002t0009g0061 a0001c0002t0009g0098 a0001c0002t0009g0099 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.729+360_729+361ins others(1): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691012 | |||||||
| chr4:169691037 | C | T | 1 | a0001c0001t0006g0191 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.729+385C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691037 | |||||||
| chr4:169691087 | G | A | 59 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(56): Show |
65 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.729+435G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691087 | |||||||
| chr4:169691185 | G | T | 1 | a0001c0001t0031g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.729+533G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691185 | |||||||
| chr4:169691189 | T | G | 46 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(43): Show |
49 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.729+537T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691189 | |||||||
| chr4:169691193 | T | G | 7 | a0001c0003t0003g0003 a0001c0003t0003g0257 a0001c0003t0003g0259 others(4): Show |
8 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.729+541T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691193 | |||||||
| chr4:169691524 | T | G | 1 | a0001c0001t0001g0160 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.730-590T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691524 | |||||||
| chr4:169691608 | G | A | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.730-506G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691608 | |||||||
| chr4:169691663 | C | T | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.730-451C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691663 | |||||||
| chr4:169691837 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.730-277A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169691837 | |||||||
| chr4:169692017 | A | G | 1 | a0001c0001t0005g0246 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.730-97A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 6/12 | chr4 | 169692017 | |||||||
| chr4:169692926 | A | G | 1 | a0001c0001t0035g0024 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.936+606A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169692926 | |||||||
| chr4:169692934 | T | C | 4 | a0001c0003t0003g0026 a0001c0003t0003g0027 a0001c0003t0003g0028 others(1): Show |
4 | HG02055.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.936+614T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169692934 | |||||||
| chr4:169692988 | A | G | 1 | a0001c0001t0025g0004 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.936+668A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169692988 | |||||||
| chr4:169693054 | G | A | 3 | a0001c0003t0003g0026 a0001c0003t0003g0027 a0001c0003t0003g0028 |
3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.936+734G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169693054 | |||||||
| chr4:169693581 | AT | A | 50 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(47): Show |
56 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.936+1263delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 169693581 | ||||||
| chr4:169693899 | G | A | 1 | a0001c0002t0002g0072 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.936+1579G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169693899 | |||||||
| chr4:169693944 | G | A | 2 | a0001c0003t0020g0179 a0001c0003t0020g0180 |
2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.936+1624G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169693944 | |||||||
| chr4:169694182 | A | G | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.937-1430A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694182 | |||||||
| chr4:169694197 | C | T | 260 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(257): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.937-1415C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694197 | |||||||
| chr4:169694274 | A | C | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.937-1338A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694274 | |||||||
| chr4:169694352 | C | T | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.937-1260C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694352 | |||||||
| chr4:169694372 | G | C | 22 | a0001c0003t0004g0006 a0001c0003t0004g0043 a0001c0003t0004g0044 others(19): Show |
23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.937-1240G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694372 | |||||||
| chr4:169694386 | A | G | 1 | a0001c0003t0004g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.937-1226A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694386 | |||||||
| chr4:169694500 | C | A | 7 | a0001c0002t0002g0069 a0001c0002t0002g0081 a0001c0002t0002g0092 others(4): Show |
7 | HG00558.hp1 HG02155.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.937-1112C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694500 | |||||||
| chr4:169694700 | G | A | 33 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(30): Show |
33 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.937-912G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694700 | |||||||
| chr4:169694711 | C | T | 1 | a0001c0001t0006g0191 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.937-901C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694711 | |||||||
| chr4:169694818 | A | G | 254 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(251): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.937-794A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169694818 | |||||||
| chr4:169695054 | A | G | 2 | a0001c0003t0004g0044 a0001c0003t0004g0046 |
2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.937-558A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169695054 | |||||||
| chr4:169695314 | C | T | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
95 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.937-298C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169695314 | |||||||
| chr4:169695346 | T | C | 1 | a0001c0001t0024g0210 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.937-266T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169695346 | |||||||
| chr4:169695423 | A | C | 1 | a0001c0001t0035g0024 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.937-189A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169695423 | |||||||
| chr4:169695424 | A | G | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.937-188A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169695424 | |||||||
| chr4:169695564 | T | C | 22 | a0001c0003t0004g0006 a0001c0003t0004g0043 a0001c0003t0004g0044 others(19): Show |
23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.937-48T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 7/12 | chr4 | 169695564 | |||||||
| chr4:169695767 | G | A | 260 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(257): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1017+75G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169695767 | |||||||
| chr4:169695924 | A | G | 9 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(6): Show |
9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1017+232A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169695924 | |||||||
| chr4:169695957 | G | A | 3 | a0001c0003t0003g0023 a0001c0003t0003g0033 a0001c0003t0003g0034 |
3 | NA18982.hp1 NA18984.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1017+265G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169695957 | |||||||
| chr4:169696003 | A | G | 60 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(57): Show |
66 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1017+311A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169696003 | |||||||
| chr4:169696095 | G | T | 1 | a0001c0003t0023g0045 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1017+403G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169696095 | |||||||
| chr4:169696176 | G | A | 2 | a0001c0001t0001g0178 a0001c0001t0001g0182 |
2 | HG00609.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1017+484G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169696176 | |||||||
| chr4:169696180 | C | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0129 |
3 | HG00280.hp2 HG01175.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1017+488C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169696180 | |||||||
| chr4:169696613 | C | T | 1 | a0001c0001t0034g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1018-576C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169696613 | |||||||
| chr4:169696626 | A | G | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.1018-563A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169696626 | |||||||
| chr4:169696819 | T | TC | 46 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(43): Show |
49 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(46): Show |
intron_variant | MODIFIER | c.1018-370_1018-369i others(3): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169696819 | |||||||
| chr4:169696907 | A | T | 4 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(1): Show |
4 | HG02622.hp1 HG02630.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1018-282A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 8/12 | chr4 | 169696907 | |||||||
| chr4:169698037 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1563+303T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169698037 | |||||||
| chr4:169698246 | A | G | 1 | a0001c0001t0005g0246 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1563+512A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169698246 | |||||||
| chr4:169698365 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0163 |
3 | HG00558.hp2 HG02040.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1563+631A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169698365 | |||||||
| chr4:169698398 | G | A | 1 | a0001c0002t0008g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1563+664G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169698398 | |||||||
| chr4:169698419 | C | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0129 |
3 | HG00280.hp2 HG01175.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1563+685C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169698419 | |||||||
| chr4:169698526 | C | A | 4 | a0001c0001t0012g0247 a0001c0001t0012g0250 a0001c0001t0012g0252 others(1): Show |
4 | HG02486.hp2 HG03540.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1563+792C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169698526 | |||||||
| chr4:169698734 | T | C | 22 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(19): Show |
27 | HG00597.hp1 HG00609.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.1563+1000T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169698734 | |||||||
| chr4:169699030 | TCTC | T | 3 | a0001c0002t0002g0065 a0001c0002t0002g0082 a0001c0002t0041g0102 |
3 | HG00140.hp2 HG01106.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1563+1299_1563+130 others(7): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 169699030 | ||||||
| chr4:169699099 | G | A | 3 | a0001c0001t0001g0177 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | NA18981.hp2 NA18986.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1563+1365G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169699099 | |||||||
| chr4:169699377 | G | A | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1563+1643G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169699377 | |||||||
| chr4:169699661 | A | G | 64 | a0001c0001t0033g0267 a0001c0001t0042g0256 a0001c0001t0045g0268 others(61): Show |
70 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1563+1927A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169699661 | |||||||
| chr4:169699720 | A | G | 7 | a0001c0003t0003g0003 a0001c0003t0003g0257 a0001c0003t0003g0259 others(4): Show |
8 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1563+1986A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169699720 | |||||||
| chr4:169699775 | G | A | 17 | a0001c0003t0003g0005 a0001c0003t0003g0023 a0001c0003t0003g0026 others(14): Show |
18 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.1563+2041G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169699775 | |||||||
| chr4:169699874 | A | G | 1 | a0001c0003t0003g0036 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1563+2140A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169699874 | |||||||
| chr4:169699894 | T | G | 64 | a0001c0001t0001g0231 a0001c0001t0015g0015 a0001c0001t0015g0184 others(61): Show |
71 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1563+2160T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169699894 | |||||||
| chr4:169699997 | G | T | 1 | a0001c0001t0035g0024 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1563+2263G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169699997 | |||||||
| chr4:169700081 | C | T | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.1563+2347C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169700081 | |||||||
| chr4:169700252 | A | AGTTT | 144 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(141): Show |
153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.1563+2522_1563+252 others(8): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 169700252 | ||||||
| chr4:169700536 | A | G | 9 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(6): Show |
9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1563+2802A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169700536 | |||||||
| chr4:169700817 | G | A | 1 | a0001c0001t0034g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1563+3083G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169700817 | |||||||
| chr4:169700822 | A | G | 87 | a0001c0001t0025g0004 a0001c0001t0033g0267 a0001c0001t0042g0256 others(84): Show |
95 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1563+3088A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169700822 | |||||||
| chr4:169700890 | G | T | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1564-3108G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169700890 | |||||||
| chr4:169700906 | G | T | 4 | a0001c0003t0003g0026 a0001c0003t0003g0027 a0001c0003t0003g0028 others(1): Show |
4 | HG02055.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1564-3092G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169700906 | |||||||
| chr4:169701042 | CTCTGTAG others(2): Show |
C | 3 | a0001c0003t0003g0023 a0001c0003t0003g0033 a0001c0003t0003g0034 |
3 | NA18982.hp1 NA18984.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1564-2954_1564-294 others(13): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 169701042 | ||||||
| chr4:169701044 | CTGTAGCA | C | 21 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0026 others(18): Show |
23 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.1564-2950_1564-294 others(11): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 169701044 | ||||||
| chr4:169701071 | A | C | 1 | a0001c0002t0017g0008 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1564-2927A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169701071 | |||||||
| chr4:169701278 | T | A | 5 | a0001c0002t0002g0001 a0001c0002t0002g0064 a0001c0002t0002g0070 others(2): Show |
7 | NA18940.hp2 NA18943.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1564-2720T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169701278 | |||||||
| chr4:169701344 | T | G | 2 | a0001c0001t0001g0151 a0001c0001t0001g0167 |
2 | HG01074.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1564-2654T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169701344 | |||||||
| chr4:169701453 | C | A | 1 | a0001c0001t0001g0231 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1564-2545C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169701453 | |||||||
| chr4:169701773 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1564-2225C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169701773 | |||||||
| chr4:169701850 | A | G | 3 | a0001c0003t0003g0023 a0001c0003t0003g0033 a0001c0003t0003g0034 |
3 | NA18982.hp1 NA18984.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1564-2148A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169701850 | |||||||
| chr4:169702068 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1564-1930G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702068 | |||||||
| chr4:169702076 | C | T | 1 | a0001c0002t0041g0102 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1564-1922C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702076 | |||||||
| chr4:169702083 | C | T | 2 | a0001c0001t0015g0015 a0001c0001t0015g0184 |
3 | HG02615.hp2 HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1564-1915C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702083 | |||||||
| chr4:169702087 | C | T | 1 | a0001c0001t0010g0216 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1564-1911C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702087 | |||||||
| chr4:169702091 | C | A | 1 | a0001c0003t0004g0053 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1564-1907C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702091 | |||||||
| chr4:169702142 | G | T | 3 | a0001c0001t0005g0244 a0001c0001t0005g0245 a0001c0001t0005g0246 |
3 | HG02622.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1564-1856G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702142 | |||||||
| chr4:169702403 | G | A | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.1564-1595G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702403 | |||||||
| chr4:169702679 | C | T | 6 | a0001c0001t0005g0017 a0001c0001t0005g0238 a0001c0001t0005g0239 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1564-1319C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702679 | |||||||
| chr4:169702777 | C | CA | 24 | a0001c0001t0011g0185 a0001c0001t0012g0250 a0001c0001t0024g0210 others(21): Show |
25 | HG01346.hp1 HG01981.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1564-1201dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 169702777 | ||||||
| chr4:169702777 | C | CAA | 56 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(53): Show |
59 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1564-1202_1564-120 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 169702777 | ||||||
| chr4:169702777 | CAAAAAAA others(5): Show |
C | 89 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(86): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1564-1212_1564-120 others(16): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 169702777 | ||||||
| chr4:169702795 | A | G | 63 | a0001c0001t0033g0267 a0001c0001t0042g0256 a0001c0001t0045g0268 others(60): Show |
69 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1564-1203A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702795 | |||||||
| chr4:169702831 | C | G | 61 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(58): Show |
67 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1564-1167C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702831 | |||||||
| chr4:169702864 | C | T | 1 | a0001c0002t0002g0095 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1564-1134C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169702864 | |||||||
| chr4:169703179 | T | C | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.1564-819T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169703179 | |||||||
| chr4:169703225 | G | T | 1 | a0001c0001t0001g0116 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1564-773G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169703225 | |||||||
| chr4:169703629 | A | G | 9 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(6): Show |
9 | HG01884.hp1 HG02572.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1564-369A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169703629 | |||||||
| chr4:169703664 | C | CT | 47 | a0001c0001t0025g0004 a0001c0003t0003g0003 a0001c0003t0003g0005 others(44): Show |
51 | HG00639.hp2 HG01175.hp2 HG01346.hp1 others(48): Show |
intron_variant | MODIFIER | c.1564-324dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr4 | 169703664 | ||||||
| chr4:169703947 | G | A | 1 | a0001c0001t0006g0189 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1564-51G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 9/12 | chr4 | 169703947 | |||||||
| chr4:169704241 | G | A | 1 | a0001c0001t0043g0248 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1750+57G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169704241 | |||||||
| chr4:169704298 | G | A | 1 | a0001c0001t0044g0222 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1750+114G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169704298 | |||||||
| chr4:169704325 | G | A | 1 | a0001c0002t0002g0103 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1750+141G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169704325 | |||||||
| chr4:169704483 | C | G | 1 | a0001c0001t0010g0230 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1750+299C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169704483 | |||||||
| chr4:169704492 | C | G | 1 | a0001c0002t0051g0041 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1750+308C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169704492 | |||||||
| chr4:169705149 | G | T | 6 | a0001c0003t0003g0003 a0001c0003t0003g0257 a0001c0003t0003g0259 others(3): Show |
7 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1750+965G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169705149 | |||||||
| chr4:169705240 | C | T | 24 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(21): Show |
26 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.1750+1056C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169705240 | |||||||
| chr4:169705269 | A | G | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1750+1085A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169705269 | |||||||
| chr4:169705401 | T | C | 91 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(88): Show |
97 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1750+1217T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169705401 | |||||||
| chr4:169705690 | T | C | 7 | a0001c0003t0004g0006 a0001c0003t0004g0054 a0001c0003t0004g0056 others(4): Show |
8 | HG00639.hp2 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1751-1178T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169705690 | |||||||
| chr4:169705747 | C | T | 62 | a0001c0001t0042g0256 a0001c0002t0002g0001 a0001c0002t0002g0002 others(59): Show |
68 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1751-1121C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169705747 | |||||||
| chr4:169705776 | C | T | 6 | a0001c0001t0006g0189 a0001c0001t0006g0190 a0001c0001t0006g0191 others(3): Show |
6 | HG01884.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1751-1092C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169705776 | |||||||
| chr4:169705894 | G | A | 8 | a0001c0001t0007g0206 a0001c0001t0007g0209 a0001c0001t0011g0185 others(5): Show |
9 | HG00323.hp2 HG00733.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1751-974G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169705894 | |||||||
| chr4:169705968 | C | G | 6 | a0001c0001t0013g0225 a0001c0001t0013g0229 a0001c0001t0013g0249 others(3): Show |
6 | HG01099.hp1 HG01433.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1751-900C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169705968 | |||||||
| chr4:169706071 | G | A | 1 | a0001c0003t0023g0045 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1751-797G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169706071 | |||||||
| chr4:169706132 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0155 |
2 | HG02027.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1751-736G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169706132 | |||||||
| chr4:169706181 | A | G | 1 | a0001c0001t0034g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1751-687A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169706181 | |||||||
| chr4:169706293 | C | T | 1 | a0001c0001t0035g0024 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1751-575C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169706293 | |||||||
| chr4:169706464 | TTTG | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0163 |
3 | HG00558.hp2 HG02040.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1751-402_1751-400d others(5): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 169706464 | ||||||
| chr4:169706624 | G | C | 4 | a0001c0003t0003g0026 a0001c0003t0003g0027 a0001c0003t0003g0028 others(1): Show |
4 | HG02055.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1751-244G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169706624 | |||||||
| chr4:169706760 | C | T | 1 | a0001c0003t0003g0260 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1751-108C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 10/12 | chr4 | 169706760 | |||||||
| chr4:169707323 | A | G | 92 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(89): Show |
98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.2149+57A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169707323 | |||||||
| chr4:169707373 | A | G | 144 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(141): Show |
153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.2149+107A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169707373 | |||||||
| chr4:169707463 | A | G | 1 | a0001c0001t0034g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2149+197A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169707463 | |||||||
| chr4:169707600 | G | T | 2 | a0001c0003t0022g0199 a0001c0003t0022g0200 |
2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2149+334G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169707600 | |||||||
| chr4:169707883 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2149+617A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169707883 | |||||||
| chr4:169708583 | C | T | 1 | a0001c0001t0001g0014 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2149+1317C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169708583 | |||||||
| chr4:169709095 | T | G | 1 | a0001c0001t0052g0040 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2149+1829T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169709095 | |||||||
| chr4:169709308 | C | T | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2149+2042C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169709308 | |||||||
| chr4:169709331 | T | C | 269 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(266): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.2149+2065T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169709331 | |||||||
| chr4:169709382 | T | TA | 29 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(26): Show |
31 | HG01175.hp2 HG01346.hp1 HG01516.hp2 others(28): Show |
intron_variant | MODIFIER | c.2149+2129dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 169709382 | ||||||
| chr4:169709554 | G | A | 25 | a0001c0001t0034g0233 a0001c0003t0003g0003 a0001c0003t0003g0005 others(22): Show |
27 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.2149+2288G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169709554 | |||||||
| chr4:169709589 | G | A | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2149+2323G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169709589 | |||||||
| chr4:169709644 | A | T | 33 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(30): Show |
33 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.2149+2378A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169709644 | |||||||
| chr4:169709677 | C | CA | 27 | a0001c0001t0001g0014 a0001c0001t0010g0228 a0001c0001t0021g0219 others(24): Show |
30 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.2149+2424dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 169709677 | ||||||
| chr4:169709949 | TTGTC | T | 33 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(30): Show |
33 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.2149+2686_2149+268 others(8): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 169709949 | ||||||
| chr4:169709995 | G | A | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.2149+2729G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169709995 | |||||||
| chr4:169710201 | G | T | 1 | a0001c0001t0001g0254 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2150-2878G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169710201 | |||||||
| chr4:169710559 | C | T | 1 | a0001c0001t0001g0010 | 2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2150-2520C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169710559 | |||||||
| chr4:169710690 | T | G | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2150-2389T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169710690 | |||||||
| chr4:169710765 | A | G | 4 | a0001c0002t0008g0196 a0001c0002t0008g0197 a0001c0002t0008g0198 others(1): Show |
4 | HG02809.hp2 HG02965.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-2314A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169710765 | |||||||
| chr4:169710777 | A | T | 4 | a0001c0003t0003g0031 a0001c0003t0003g0035 a0001c0003t0003g0036 others(1): Show |
4 | HG01981.hp1 NA18989.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-2302A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169710777 | |||||||
| chr4:169710879 | G | C | 1 | a0001c0001t0013g0225 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2150-2200G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169710879 | |||||||
| chr4:169710968 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2150-2111A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169710968 | |||||||
| chr4:169711105 | T | C | 2 | a0001c0001t0010g0201 a0001c0001t0016g0203 |
2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2150-1974T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169711105 | |||||||
| chr4:169711155 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2150-1924G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169711155 | |||||||
| chr4:169711331 | A | G | 62 | a0001c0001t0042g0256 a0001c0002t0002g0001 a0001c0002t0002g0002 others(59): Show |
68 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2150-1748A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169711331 | |||||||
| chr4:169711512 | A | G | 255 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(252): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.2150-1567A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169711512 | |||||||
| chr4:169711570 | G | A | 1 | a0001c0007t0001g0158 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2150-1509G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169711570 | |||||||
| chr4:169711869 | T | A | 60 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(57): Show |
62 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.2150-1210T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169711869 | |||||||
| chr4:169711884 | C | T | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.2150-1195C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169711884 | |||||||
| chr4:169711900 | T | G | 4 | a0001c0003t0003g0031 a0001c0003t0003g0035 a0001c0003t0003g0036 others(1): Show |
4 | HG01981.hp1 NA18989.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.2150-1179T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169711900 | |||||||
| chr4:169711958 | G | A | 1 | a0001c0002t0002g0091 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2150-1121G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169711958 | |||||||
| chr4:169712021 | A | AT | 24 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0127 others(21): Show |
24 | HG01106.hp1 HG01106.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.2150-1036dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 169712021 | ||||||
| chr4:169712021 | A | ATT | 25 | a0001c0001t0001g0157 a0001c0001t0042g0256 a0001c0002t0002g0072 others(22): Show |
27 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.2150-1037_2150-103 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 169712021 | ||||||
| chr4:169712021 | AT | A | 7 | a0001c0001t0001g0115 a0001c0001t0001g0128 a0001c0001t0001g0130 others(4): Show |
7 | HG02451.hp2 HG02572.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.2150-1036delT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 169712021 | ||||||
| chr4:169712021 | ATTTTTTT | A | 33 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(30): Show |
33 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.2150-1042_2150-103 others(11): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 169712021 | ||||||
| chr4:169712071 | A | C | 146 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(143): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.2150-1008A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169712071 | |||||||
| chr4:169712300 | C | A | 25 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(22): Show |
27 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.2150-779C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169712300 | |||||||
| chr4:169712574 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0019g0126 |
2 | HG01496.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2150-505A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169712574 | |||||||
| chr4:169712730 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2150-349C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169712730 | |||||||
| chr4:169712760 | C | G | 1 | a0001c0003t0037g0050 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2150-319C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 11/12 | chr4 | 169712760 | |||||||
| chr4:169713400 | G | A | 10 | a0001c0003t0004g0044 a0001c0003t0004g0046 a0001c0003t0004g0047 others(7): Show |
10 | HG01175.hp2 HG01358.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2366+105G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169713400 | |||||||
| chr4:169713503 | C | T | 2 | a0001c0001t0033g0267 a0001c0001t0045g0268 |
2 | HG03579.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2366+208C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169713503 | |||||||
| chr4:169713552 | G | T | 1 | a0001c0001t0034g0233 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2366+257G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169713552 | |||||||
| chr4:169713875 | T | G | 1 | a0001c0001t0025g0004 | 2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2366+580T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169713875 | |||||||
| chr4:169713953 | A | G | 61 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(58): Show |
67 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2366+658A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169713953 | |||||||
| chr4:169714046 | A | G | 19 | a0001c0001t0025g0004 a0001c0001t0052g0040 a0001c0003t0004g0006 others(16): Show |
21 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.2366+751A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714046 | |||||||
| chr4:169714167 | C | T | 2 | a0001c0001t0007g0206 a0001c0001t0007g0209 |
2 | HG00323.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.2366+872C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714167 | |||||||
| chr4:169714238 | G | A | 3 | a0001c0003t0003g0023 a0001c0003t0003g0033 a0001c0003t0003g0034 |
3 | NA18982.hp1 NA18984.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2366+943G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714238 | |||||||
| chr4:169714261 | CAG | C | 4 | a0001c0002t0008g0196 a0001c0002t0008g0197 a0001c0002t0008g0198 others(1): Show |
4 | HG02809.hp2 HG02965.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2366+970_2366+971d others(4): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 169714261 | ||||||
| chr4:169714286 | G | GT | 55 | a0001c0001t0006g0189 a0001c0001t0012g0247 a0001c0001t0012g0250 others(52): Show |
61 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.2366+1003dupT | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 169714286 | ||||||
| chr4:169714339 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2366+1044T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714339 | |||||||
| chr4:169714430 | C | G | 1 | a0001c0003t0003g0037 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2366+1135C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714430 | |||||||
| chr4:169714439 | G | A | 25 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(22): Show |
27 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.2366+1144G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714439 | |||||||
| chr4:169714453 | C | A | 89 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(86): Show |
94 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.2366+1158C>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714453 | |||||||
| chr4:169714485 | A | G | 34 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(31): Show |
34 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.2366+1190A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714485 | |||||||
| chr4:169714730 | C | T | 22 | a0001c0003t0004g0006 a0001c0003t0004g0043 a0001c0003t0004g0044 others(19): Show |
23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.2366+1435C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714730 | |||||||
| chr4:169714906 | T | C | 2 | a0001c0001t0005g0242 a0001c0001t0005g0243 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2366+1611T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169714906 | |||||||
| chr4:169715312 | C | T | 3 | a0001c0002t0002g0063 a0001c0002t0002g0071 a0001c0002t0002g0072 |
3 | HG01978.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2366+2017C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169715312 | |||||||
| chr4:169715414 | A | G | 22 | a0001c0003t0004g0006 a0001c0003t0004g0043 a0001c0003t0004g0044 others(19): Show |
23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.2366+2119A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169715414 | |||||||
| chr4:169715494 | G | A | 1 | a0001c0001t0035g0024 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2366+2199G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169715494 | |||||||
| chr4:169715748 | T | C | 23 | a0001c0001t0025g0004 a0001c0003t0004g0006 a0001c0003t0004g0043 others(20): Show |
25 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.2366+2453T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169715748 | |||||||
| chr4:169715821 | G | GA | 255 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(252): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.2366+2532dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 169715821 | ||||||
| chr4:169715902 | G | C | 1 | a0001c0001t0042g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2366+2607G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169715902 | |||||||
| chr4:169716119 | C | G | 2 | a0001c0003t0020g0179 a0001c0003t0020g0180 |
2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2366+2824C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169716119 | |||||||
| chr4:169716367 | C | T | 25 | a0001c0003t0003g0003 a0001c0003t0003g0005 a0001c0003t0003g0023 others(22): Show |
27 | HG01346.hp1 HG01516.hp2 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.2366+3072C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169716367 | |||||||
| chr4:169716421 | C | G | 1 | a0001c0002t0008g0196 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2366+3126C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169716421 | |||||||
| chr4:169716515 | T | TA | 22 | a0001c0003t0004g0006 a0001c0003t0004g0043 a0001c0003t0004g0044 others(19): Show |
23 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(20): Show |
intron_variant | MODIFIER | c.2366+3228dupA | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 169716515 | ||||||
| chr4:169716959 | T | A | 5 | a0001c0002t0009g0061 a0001c0002t0009g0098 a0001c0002t0009g0099 others(2): Show |
5 | HG02109.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2367-2948T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169716959 | |||||||
| chr4:169717101 | A | G | 1 | a0001c0001t0006g0192 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2367-2806A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169717101 | |||||||
| chr4:169717197 | C | G | 1 | a0001c0001t0001g0161 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2367-2710C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169717197 | |||||||
| chr4:169717265 | A | G | 5 | a0001c0001t0001g0140 a0001c0001t0001g0142 a0001c0001t0001g0143 others(2): Show |
5 | HG01192.hp1 HG03491.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.2367-2642A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169717265 | |||||||
| chr4:169717315 | C | T | 80 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(77): Show |
84 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.2367-2592C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169717315 | |||||||
| chr4:169717390 | G | T | 2 | a0001c0003t0020g0179 a0001c0003t0020g0180 |
2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2367-2517G>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169717390 | |||||||
| chr4:169717740 | ACT | A | 62 | a0001c0001t0042g0256 a0001c0002t0002g0001 a0001c0002t0002g0002 others(59): Show |
68 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.2367-2164_2367-216 others(6): Show |
CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr4 | 169717740 | ||||||
| chr4:169717741 | C | G | 6 | a0001c0001t0005g0017 a0001c0001t0005g0238 a0001c0001t0005g0239 others(3): Show |
6 | HG01109.hp1 HG02258.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2367-2166C>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169717741 | |||||||
| chr4:169717983 | A | G | 1 | a0001c0001t0030g0237 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2367-1924A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169717983 | |||||||
| chr4:169718267 | T | C | 2 | a0001c0003t0022g0199 a0001c0003t0022g0200 |
2 | HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2367-1640T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169718267 | |||||||
| chr4:169718299 | T | C | 61 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0007 others(58): Show |
67 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2367-1608T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169718299 | |||||||
| chr4:169718470 | T | A | 1 | a0001c0003t0003g0032 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2367-1437T>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169718470 | |||||||
| chr4:169718825 | G | A | 2 | a0001c0003t0020g0179 a0001c0003t0020g0180 |
2 | HG02886.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2367-1082G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169718825 | |||||||
| chr4:169718906 | A | G | 1 | a0001c0003t0004g0049 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2367-1001A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169718906 | |||||||
| chr4:169718941 | A | C | 1 | a0001c0002t0002g0103 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2367-966A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169718941 | |||||||
| chr4:169719003 | A | T | 84 | a0001c0001t0042g0256 a0001c0002t0002g0001 a0001c0002t0002g0002 others(81): Show |
91 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.2367-904A>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719003 | |||||||
| chr4:169719094 | G | A | 1 | a0001c0001t0013g0225 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2367-813G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719094 | |||||||
| chr4:169719256 | G | A | 1 | a0001c0001t0052g0040 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2367-651G>A | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719256 | |||||||
| chr4:169719270 | T | G | 145 | a0001c0001t0007g0204 a0001c0001t0007g0205 a0001c0001t0007g0206 others(142): Show |
154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.2367-637T>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719270 | |||||||
| chr4:169719395 | C | T | 1 | a0001c0006t0046g0212 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2367-512C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719395 | |||||||
| chr4:169719567 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2367-340A>G | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719567 | |||||||
| chr4:169719640 | A | C | 23 | a0001c0001t0025g0004 a0001c0003t0004g0006 a0001c0003t0004g0043 others(20): Show |
25 | HG00639.hp2 HG01175.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.2367-267A>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719640 | |||||||
| chr4:169719668 | G | C | 1 | a0001c0001t0001g0177 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2367-239G>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719668 | |||||||
| chr4:169719842 | T | C | 85 | a0001c0001t0025g0004 a0001c0001t0042g0256 a0001c0002t0002g0001 others(82): Show |
93 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.2367-65T>C | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719842 | |||||||
| chr4:169719899 | C | T | 2 | a0001c0003t0022g0199 a0001c0003t0022g0200 |
2 | HG02723.hp2 HG03041.hp2 |
splice_region_variant&intron_variant | LOW | c.2367-8C>T | CLCN3 | ENSG00000109572.16 | transcript | ENST00000513761.6 | protein_coding | 12/12 | chr4 | 169719899 |